List of Excipients in API ibuprofen and famotidine
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Excipients in NDA-approved (novel) drugs containing ibuprofen and famotidine
| Company | Tradename | Ingredient | NDC | Excipient | Potential Generic Entry |
|---|---|---|---|---|---|
| Lupin Pharmaceuticals Inc | IBUPROFEN AND FAMOTIDINE | ibuprofen and famotidine | 70748-312 | CELLULOSE, MICROCRYSTALLINE | |
| Lupin Pharmaceuticals Inc | IBUPROFEN AND FAMOTIDINE | ibuprofen and famotidine | 70748-312 | CROSCARMELLOSE SODIUM | |
| Lupin Pharmaceuticals Inc | IBUPROFEN AND FAMOTIDINE | ibuprofen and famotidine | 70748-312 | FD&C BLUE NO. 1 | |
| Lupin Pharmaceuticals Inc | IBUPROFEN AND FAMOTIDINE | ibuprofen and famotidine | 70748-312 | FD&C BLUE NO. 2--ALUMINUM LAKE | |
| Lupin Pharmaceuticals Inc | IBUPROFEN AND FAMOTIDINE | ibuprofen and famotidine | 70748-312 | HYPROMELLOSE | |
| Lupin Pharmaceuticals Inc | IBUPROFEN AND FAMOTIDINE | ibuprofen and famotidine | 70748-312 | LACTOSE | |
| >Company | >Tradename | >Ingredient | >NDC | >Excipient | >Potential Generic Entry |
Excipients in ANDA-approved (generic) drugs containing ibuprofen and famotidine
Detailed excipient profiles for ibuprofen and famotidine
Excipient focus: AMMONIA
ibuprofen and famotidine drug variants containing AMMONIA
ibuprofen and famotidine drug variants not containing AMMONIA
Excipient focus: ANHYDROUS LACTOSE
ibuprofen and famotidine drug variants containing ANHYDROUS LACTOSE
| Company | Ingredient | NDC |
|---|---|---|
| ENDO USA Inc | ibuprofen and famotidine | 49884-366 |
| Advanced Rx of Tennessee LLC | ibuprofen and famotidine | 80425-0483 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing ANHYDROUS LACTOSE
Excipient focus: CELLULOSE, MICROCRYSTALLINE
ibuprofen and famotidine drug variants containing CELLULOSE, MICROCRYSTALLINE
ibuprofen and famotidine drug variants not containing CELLULOSE, MICROCRYSTALLINE
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: CROSCARMELLOSE SODIUM
ibuprofen and famotidine drug variants containing CROSCARMELLOSE SODIUM
ibuprofen and famotidine drug variants not containing CROSCARMELLOSE SODIUM
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: FD&C BLUE NO. 1
ibuprofen and famotidine drug variants containing FD&C BLUE NO. 1
ibuprofen and famotidine drug variants not containing FD&C BLUE NO. 1
Excipient focus: FD&C BLUE NO. 1 ALUMINUM LAKE
ibuprofen and famotidine drug variants containing FD&C BLUE NO. 1 ALUMINUM LAKE
| Company | Ingredient | NDC |
|---|---|---|
| ENDO USA Inc | ibuprofen and famotidine | 49884-366 |
| Advanced Rx of Tennessee LLC | ibuprofen and famotidine | 80425-0483 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing FD&C BLUE NO. 1 ALUMINUM LAKE
Excipient focus: FD&C BLUE NO. 2
ibuprofen and famotidine drug variants containing FD&C BLUE NO. 2
ibuprofen and famotidine drug variants not containing FD&C BLUE NO. 2
Excipient focus: FD&C BLUE NO. 2 ALUMINUM LAKE
ibuprofen and famotidine drug variants containing FD&C BLUE NO. 2 ALUMINUM LAKE
| Company | Ingredient | NDC |
|---|---|---|
| Horizon Therapeutics USA Inc | ibuprofen and famotidine | 75987-010 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing FD&C BLUE NO. 2 ALUMINUM LAKE
Excipient focus: FD&C BLUE NO. 2--ALUMINUM LAKE
ibuprofen and famotidine drug variants containing FD&C BLUE NO. 2--ALUMINUM LAKE
| Company | Ingredient | NDC |
|---|---|---|
| Teva Pharmaceuticals USA Inc | ibuprofen and famotidine | 0093-8107 |
| ENDO USA Inc | ibuprofen and famotidine | 49884-366 |
| Lupin Pharmaceuticals Inc | ibuprofen and famotidine | 70748-312 |
| Advanced Rx of Tennessee LLC | ibuprofen and famotidine | 80425-0483 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing FD&C BLUE NO. 2--ALUMINUM LAKE
Excipient focus: FERROSOFERRIC OXIDE
ibuprofen and famotidine drug variants containing FERROSOFERRIC OXIDE
ibuprofen and famotidine drug variants not containing FERROSOFERRIC OXIDE
Excipient focus: GLYCERIN
ibuprofen and famotidine drug variants containing GLYCERIN
| Company | Ingredient | NDC |
|---|---|---|
| Camber Pharmaceuticals Inc | ibuprofen and famotidine | 31722-315 |
| Ascent Pharmaceuticals Inc | ibuprofen and famotidine | 43602-544 |
| Advanced Rx Pharmacy of Tennessee LLC | ibuprofen and famotidine | 80425-0384 |
| PHOENIX RX LLC | ibuprofen and famotidine | 85509-1315 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing GLYCERIN
Excipient focus: GLYCERYL MONO- AND DICAPRYLOCAPRATE
ibuprofen and famotidine drug variants containing GLYCERYL MONO- AND DICAPRYLOCAPRATE
| Company | Ingredient | NDC |
|---|---|---|
| Zydus Lifesciences Limited | ibuprofen and famotidine | 70771-1924 |
| Viona Pharmaceuticals Inc | ibuprofen and famotidine | 72578-214 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing GLYCERYL MONO- AND DICAPRYLOCAPRATE
Excipient focus: HYDROXYPROPYL CELLULOSE
ibuprofen and famotidine drug variants containing HYDROXYPROPYL CELLULOSE
ibuprofen and famotidine drug variants not containing HYDROXYPROPYL CELLULOSE
Excipient focus: HYPROMELLOSE
ibuprofen and famotidine drug variants containing HYPROMELLOSE
ibuprofen and famotidine drug variants not containing HYPROMELLOSE
Excipient focus: HYPROMELLOSE 2910
ibuprofen and famotidine drug variants containing HYPROMELLOSE 2910
| Company | Ingredient | NDC |
|---|---|---|
| Teva Pharmaceuticals USA Inc | ibuprofen and famotidine | 0093-8107 |
| Zydus Lifesciences Limited | ibuprofen and famotidine | 70771-1924 |
| Viona Pharmaceuticals Inc | ibuprofen and famotidine | 72578-214 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing HYPROMELLOSE 2910
Excipient focus: LACTOSE
ibuprofen and famotidine drug variants containing LACTOSE
| Company | Ingredient | NDC |
|---|---|---|
| Lupin Pharmaceuticals Inc | ibuprofen and famotidine | 70748-312 |
| Horizon Therapeutics USA Inc | ibuprofen and famotidine | 75987-010 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing LACTOSE
Excipient focus: LACTOSE MONOHYDRATE
ibuprofen and famotidine drug variants containing LACTOSE MONOHYDRATE
| Company | Ingredient | NDC |
|---|---|---|
| Teva Pharmaceuticals USA Inc | ibuprofen and famotidine | 0093-8107 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing LACTOSE MONOHYDRATE
Excipient focus: MAGNESIUM STEARATE
ibuprofen and famotidine drug variants containing MAGNESIUM STEARATE
ibuprofen and famotidine drug variants not containing MAGNESIUM STEARATE
Excipient focus: PALMITIC ACID
ibuprofen and famotidine drug variants containing PALMITIC ACID
| Company | Ingredient | NDC |
|---|---|---|
| Aurobindo Pharma Limited | ibuprofen and famotidine | 59651-908 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing PALMITIC ACID
Excipient focus: POLYETHYLENE GLYCOL
ibuprofen and famotidine drug variants containing POLYETHYLENE GLYCOL
ibuprofen and famotidine drug variants not containing POLYETHYLENE GLYCOL
Excipient focus: POLYETHYLENE GLYCOL 3350
ibuprofen and famotidine drug variants containing POLYETHYLENE GLYCOL 3350
| Company | Ingredient | NDC |
|---|---|---|
| Teva Pharmaceuticals USA Inc | ibuprofen and famotidine | 0093-8107 |
| Aurobindo Pharma Limited | ibuprofen and famotidine | 59651-908 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing POLYETHYLENE GLYCOL 3350
Excipient focus: POLYETHYLENE GLYCOL 400
ibuprofen and famotidine drug variants containing POLYETHYLENE GLYCOL 400
| Company | Ingredient | NDC |
|---|---|---|
| Teva Pharmaceuticals USA Inc | ibuprofen and famotidine | 0093-8107 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing POLYETHYLENE GLYCOL 400
Excipient focus: POLYETHYLENE GLYCOL 8000
ibuprofen and famotidine drug variants containing POLYETHYLENE GLYCOL 8000
| Company | Ingredient | NDC |
|---|---|---|
| Teva Pharmaceuticals USA Inc | ibuprofen and famotidine | 0093-8107 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing POLYETHYLENE GLYCOL 8000
Excipient focus: POLYSORBATE 80
ibuprofen and famotidine drug variants containing POLYSORBATE 80
| Company | Ingredient | NDC |
|---|---|---|
| ENDO USA Inc | ibuprofen and famotidine | 49884-366 |
| Aurobindo Pharma Limited | ibuprofen and famotidine | 59651-908 |
| Horizon Therapeutics USA Inc | ibuprofen and famotidine | 75987-010 |
| Advanced Rx of Tennessee LLC | ibuprofen and famotidine | 80425-0483 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing POLYSORBATE 80
Excipient focus: POLYVINYL ALCOHOL
ibuprofen and famotidine drug variants containing POLYVINYL ALCOHOL
ibuprofen and famotidine drug variants not containing POLYVINYL ALCOHOL
Excipient focus: POVIDONE
ibuprofen and famotidine drug variants containing POVIDONE
ibuprofen and famotidine drug variants not containing POVIDONE
Excipient focus: POVIDONE K30
ibuprofen and famotidine drug variants containing POVIDONE K30
| Company | Ingredient | NDC |
|---|---|---|
| ENDO USA Inc | ibuprofen and famotidine | 49884-366 |
| Aurobindo Pharma Limited | ibuprofen and famotidine | 59651-908 |
| Advanced Rx of Tennessee LLC | ibuprofen and famotidine | 80425-0483 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing POVIDONE K30
Excipient focus: PROPYLENE GLYCOL
ibuprofen and famotidine drug variants containing PROPYLENE GLYCOL
ibuprofen and famotidine drug variants not containing PROPYLENE GLYCOL
Excipient focus: SHELLAC
ibuprofen and famotidine drug variants containing SHELLAC
ibuprofen and famotidine drug variants not containing SHELLAC
Excipient focus: SILICON DIOXIDE
ibuprofen and famotidine drug variants containing SILICON DIOXIDE
ibuprofen and famotidine drug variants not containing SILICON DIOXIDE
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: SODIUM LAURYL SULFATE
ibuprofen and famotidine drug variants containing SODIUM LAURYL SULFATE
| Company | Ingredient | NDC |
|---|---|---|
| Zydus Lifesciences Limited | ibuprofen and famotidine | 70771-1924 |
| Viona Pharmaceuticals Inc | ibuprofen and famotidine | 72578-214 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing SODIUM LAURYL SULFATE
Excipient focus: STARCH, CORN
ibuprofen and famotidine drug variants containing STARCH, CORN
| Company | Ingredient | NDC |
|---|---|---|
| Camber Pharmaceuticals Inc | ibuprofen and famotidine | 31722-315 |
| Ascent Pharmaceuticals Inc | ibuprofen and famotidine | 43602-544 |
| Advanced Rx Pharmacy of Tennessee LLC | ibuprofen and famotidine | 80425-0384 |
| PHOENIX RX LLC | ibuprofen and famotidine | 85509-1315 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing STARCH, CORN
Excipient focus: STEARIC ACID
ibuprofen and famotidine drug variants containing STEARIC ACID
| Company | Ingredient | NDC |
|---|---|---|
| Aurobindo Pharma Limited | ibuprofen and famotidine | 59651-908 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing STEARIC ACID
Excipient focus: TALC
ibuprofen and famotidine drug variants containing TALC
ibuprofen and famotidine drug variants not containing TALC
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: TITANIUM DIOXIDE
ibuprofen and famotidine drug variants containing TITANIUM DIOXIDE
ibuprofen and famotidine drug variants not containing TITANIUM DIOXIDE
| Company | Ingredient | NDC |
|---|---|---|
| Camber Pharmaceuticals Inc | ibuprofen and famotidine | 31722-315 |
| Ascent Pharmaceuticals Inc | ibuprofen and famotidine | 43602-544 |
| Advanced Rx Pharmacy of Tennessee LLC | ibuprofen and famotidine | 80425-0384 |
| PHOENIX RX LLC | ibuprofen and famotidine | 85509-1315 |
| >Company | >Ingredient | >NDC |
Excipient focus: WATER
ibuprofen and famotidine drug variants containing WATER
| Company | Ingredient | NDC |
|---|---|---|
| Lupin Pharmaceuticals Inc | ibuprofen and famotidine | 70748-312 |
| Horizon Therapeutics USA Inc | ibuprofen and famotidine | 75987-010 |
| >Company | >Ingredient | >NDC |
ibuprofen and famotidine drug variants not containing WATER
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