List of Excipients in API gefitinib
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Excipients in NDA-approved (novel) drugs containing gefitinib
| Company | Tradename | Ingredient | NDC | Excipient | Potential Generic Entry |
|---|---|---|---|---|---|
| AstraZeneca Pharmaceuticals LP | IRESSA | gefitinib | 0310-0482 | CELLULOSE, MICROCRYSTALLINE | |
| AstraZeneca Pharmaceuticals LP | IRESSA | gefitinib | 0310-0482 | CROSCARMELLOSE SODIUM | |
| AstraZeneca Pharmaceuticals LP | IRESSA | gefitinib | 0310-0482 | FERRIC OXIDE RED | |
| >Company | >Tradename | >Ingredient | >NDC | >Excipient | >Potential Generic Entry |
Excipients in ANDA-approved (generic) drugs containing gefitinib
| Company | Ingredient | NDC | Excipient |
|---|---|---|---|
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 | CELLULOSE, MICROCRYSTALLINE |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 | CROSCARMELLOSE SODIUM |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 | FERRIC OXIDE RED |
| >Company | >Ingredient | >NDC | >Excipient |
Detailed excipient profiles for gefitinib
Excipient focus: CELLULOSE, MICROCRYSTALLINE
gefitinib drug variants containing CELLULOSE, MICROCRYSTALLINE
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing CELLULOSE, MICROCRYSTALLINE
| Company | Ingredient | NDC |
|---|---|---|
| Apotex Corp | gefitinib | 60505-4512 |
| Natco Pharma USA LLC | gefitinib | 69339-168 |
| >Company | >Ingredient | >NDC |
Excipient focus: CROSCARMELLOSE SODIUM
gefitinib drug variants containing CROSCARMELLOSE SODIUM
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing CROSCARMELLOSE SODIUM
| Company | Ingredient | NDC |
|---|---|---|
| Apotex Corp | gefitinib | 60505-4512 |
| >Company | >Ingredient | >NDC |
Excipient focus: CROSPOVIDONE
gefitinib drug variants containing CROSPOVIDONE
| Company | Ingredient | NDC |
|---|---|---|
| Apotex Corp | gefitinib | 60505-4512 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing CROSPOVIDONE
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| >Company | >Ingredient | >NDC |
Excipient focus: DIMETHYLAMINOETHYL METHACRYLATE - BUTYL METHACRYLATE - METHYL METHACRYLATE COPOLYMER
gefitinib drug variants containing DIMETHYLAMINOETHYL METHACRYLATE - BUTYL METHACRYLATE - METHYL METHACRYLATE COPOLYMER
| Company | Ingredient | NDC |
|---|---|---|
| Apotex Corp | gefitinib | 60505-4512 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing DIMETHYLAMINOETHYL METHACRYLATE - BUTYL METHACRYLATE - METHYL METHACRYLATE COPOLYMER
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| >Company | >Ingredient | >NDC |
Excipient focus: FERRIC OXIDE RED
gefitinib drug variants containing FERRIC OXIDE RED
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing FERRIC OXIDE RED
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: FERRIC OXIDE YELLOW
gefitinib drug variants containing FERRIC OXIDE YELLOW
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing FERRIC OXIDE YELLOW
| Company | Ingredient | NDC |
|---|---|---|
| Apotex Corp | gefitinib | 60505-4512 |
| >Company | >Ingredient | >NDC |
Excipient focus: FERROSOFERRIC OXIDE
gefitinib drug variants containing FERROSOFERRIC OXIDE
| Company | Ingredient | NDC |
|---|---|---|
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| Qilu Pharmaceutical Co Ltd | gefitinib | 67184-0531 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing FERROSOFERRIC OXIDE
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Apotex Corp | gefitinib | 60505-4512 |
| >Company | >Ingredient | >NDC |
Excipient focus: HYPROMELLOSE
gefitinib drug variants containing HYPROMELLOSE
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing HYPROMELLOSE
| Company | Ingredient | NDC |
|---|---|---|
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| Apotex Corp | gefitinib | 60505-4512 |
| >Company | >Ingredient | >NDC |
Excipient focus: LACTOSE MONOHYDRATE
gefitinib drug variants containing LACTOSE MONOHYDRATE
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing LACTOSE MONOHYDRATE
| Company | Ingredient | NDC |
|---|---|---|
| Apotex Corp | gefitinib | 60505-4512 |
| >Company | >Ingredient | >NDC |
Excipient focus: MAGNESIUM STEARATE
gefitinib drug variants containing MAGNESIUM STEARATE
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing MAGNESIUM STEARATE
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: MICROCRYSTALLINE CELLULOSE 101
gefitinib drug variants containing MICROCRYSTALLINE CELLULOSE 101
| Company | Ingredient | NDC |
|---|---|---|
| Natco Pharma USA LLC | gefitinib | 69339-168 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing MICROCRYSTALLINE CELLULOSE 101
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| >Company | >Ingredient | >NDC |
Excipient focus: MICROCRYSTALLINE CELLULOSE 102
gefitinib drug variants containing MICROCRYSTALLINE CELLULOSE 102
| Company | Ingredient | NDC |
|---|---|---|
| Natco Pharma USA LLC | gefitinib | 69339-168 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing MICROCRYSTALLINE CELLULOSE 102
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| >Company | >Ingredient | >NDC |
Excipient focus: POLYETHYLENE GLYCOL
gefitinib drug variants containing POLYETHYLENE GLYCOL
| Company | Ingredient | NDC |
|---|---|---|
| Natco Pharma USA LLC | gefitinib | 69339-168 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing POLYETHYLENE GLYCOL
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| >Company | >Ingredient | >NDC |
Excipient focus: POLYETHYLENE GLYCOL 300
gefitinib drug variants containing POLYETHYLENE GLYCOL 300
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing POLYETHYLENE GLYCOL 300
| Company | Ingredient | NDC |
|---|---|---|
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| Apotex Corp | gefitinib | 60505-4512 |
| >Company | >Ingredient | >NDC |
Excipient focus: POLYETHYLENE GLYCOL 3350
gefitinib drug variants containing POLYETHYLENE GLYCOL 3350
| Company | Ingredient | NDC |
|---|---|---|
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| Qilu Pharmaceutical Co Ltd | gefitinib | 67184-0531 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing POLYETHYLENE GLYCOL 3350
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Apotex Corp | gefitinib | 60505-4512 |
| Natco Pharma USA LLC | gefitinib | 69339-168 |
| >Company | >Ingredient | >NDC |
Excipient focus: POLYETHYLENE GLYCOL 8000
gefitinib drug variants containing POLYETHYLENE GLYCOL 8000
| Company | Ingredient | NDC |
|---|---|---|
| Apotex Corp | gefitinib | 60505-4512 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing POLYETHYLENE GLYCOL 8000
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| >Company | >Ingredient | >NDC |
Excipient focus: POLYVINYL ALCOHOL
gefitinib drug variants containing POLYVINYL ALCOHOL
| Company | Ingredient | NDC |
|---|---|---|
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| Apotex Corp | gefitinib | 60505-4512 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing POLYVINYL ALCOHOL
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| >Company | >Ingredient | >NDC |
Excipient focus: POVIDONE
gefitinib drug variants containing POVIDONE
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing POVIDONE
| Company | Ingredient | NDC |
|---|---|---|
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| Apotex Corp | gefitinib | 60505-4512 |
| Qilu Pharmaceutical Co Ltd | gefitinib | 67184-0531 |
| >Company | >Ingredient | >NDC |
Excipient focus: POVIDONE K30
gefitinib drug variants containing POVIDONE K30
| Company | Ingredient | NDC |
|---|---|---|
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| Qilu Pharmaceutical Co Ltd | gefitinib | 67184-0531 |
| Natco Pharma USA LLC | gefitinib | 69339-168 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing POVIDONE K30
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Apotex Corp | gefitinib | 60505-4512 |
| >Company | >Ingredient | >NDC |
Excipient focus: SILICON DIOXIDE
gefitinib drug variants containing SILICON DIOXIDE
| Company | Ingredient | NDC |
|---|---|---|
| Apotex Corp | gefitinib | 60505-4512 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing SILICON DIOXIDE
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| >Company | >Ingredient | >NDC |
Excipient focus: SODIUM LAURYL SULFATE
gefitinib drug variants containing SODIUM LAURYL SULFATE
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing SODIUM LAURYL SULFATE
| Company | Ingredient | NDC |
|---|---|---|
| Apotex Corp | gefitinib | 60505-4512 |
| >Company | >Ingredient | >NDC |
Excipient focus: TALC
gefitinib drug variants containing TALC
| Company | Ingredient | NDC |
|---|---|---|
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| Apotex Corp | gefitinib | 60505-4512 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing TALC
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| >Company | >Ingredient | >NDC |
Excipient focus: TITANIUM DIOXIDE
gefitinib drug variants containing TITANIUM DIOXIDE
| Company | Ingredient | NDC |
|---|---|---|
| AstraZeneca Pharmaceuticals LP | gefitinib | 0310-0482 |
| Teva Pharmaceuticals Inc | gefitinib | 0480-4053 |
| Ingenus Pharmaceuticals LLC | gefitinib | 50742-366 |
| >Company | >Ingredient | >NDC |
gefitinib drug variants not containing TITANIUM DIOXIDE
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
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