List of Excipients in API butalbital and acetaminophen tablets
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Excipients in ANDA-approved (generic) drugs containing butalbital and acetaminophen tablets
Detailed excipient profiles for butalbital and acetaminophen tablets
Excipient focus: CELLULOSE, MICROCRYSTALLINE
butalbital and acetaminophen tablets drug variants containing CELLULOSE, MICROCRYSTALLINE
| Company | Ingredient | NDC |
|---|---|---|
| Bausch Health US LLC | butalbital and acetaminophen tablets | 0095-3000 |
| Oceanside Pharmaceuticals | butalbital and acetaminophen tablets | 68682-306 |
| >Company | >Ingredient | >NDC |
butalbital and acetaminophen tablets drug variants not containing CELLULOSE, MICROCRYSTALLINE
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: CROSCARMELLOSE SODIUM
butalbital and acetaminophen tablets drug variants containing CROSCARMELLOSE SODIUM
| Company | Ingredient | NDC |
|---|---|---|
| Bausch Health US LLC | butalbital and acetaminophen tablets | 0095-3000 |
| Oceanside Pharmaceuticals | butalbital and acetaminophen tablets | 68682-306 |
| >Company | >Ingredient | >NDC |
butalbital and acetaminophen tablets drug variants not containing CROSCARMELLOSE SODIUM
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: D&C YELLOW NO. 10
butalbital and acetaminophen tablets drug variants containing D&C YELLOW NO. 10
| Company | Ingredient | NDC |
|---|---|---|
| Bausch Health US LLC | butalbital and acetaminophen tablets | 0095-3000 |
| Oceanside Pharmaceuticals | butalbital and acetaminophen tablets | 68682-306 |
| >Company | >Ingredient | >NDC |
butalbital and acetaminophen tablets drug variants not containing D&C YELLOW NO. 10
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: FD&C RED NO. 40
butalbital and acetaminophen tablets drug variants containing FD&C RED NO. 40
| Company | Ingredient | NDC |
|---|---|---|
| Bausch Health US LLC | butalbital and acetaminophen tablets | 0095-3000 |
| Oceanside Pharmaceuticals | butalbital and acetaminophen tablets | 68682-306 |
| >Company | >Ingredient | >NDC |
butalbital and acetaminophen tablets drug variants not containing FD&C RED NO. 40
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: MAGNESIUM STEARATE
butalbital and acetaminophen tablets drug variants containing MAGNESIUM STEARATE
| Company | Ingredient | NDC |
|---|---|---|
| Bausch Health US LLC | butalbital and acetaminophen tablets | 0095-3000 |
| Oceanside Pharmaceuticals | butalbital and acetaminophen tablets | 68682-306 |
| >Company | >Ingredient | >NDC |
butalbital and acetaminophen tablets drug variants not containing MAGNESIUM STEARATE
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
Excipient focus: STARCH, CORN
butalbital and acetaminophen tablets drug variants containing STARCH, CORN
| Company | Ingredient | NDC |
|---|---|---|
| Bausch Health US LLC | butalbital and acetaminophen tablets | 0095-3000 |
| Oceanside Pharmaceuticals | butalbital and acetaminophen tablets | 68682-306 |
| >Company | >Ingredient | >NDC |
butalbital and acetaminophen tablets drug variants not containing STARCH, CORN
| Company | Ingredient | NDC |
|---|---|---|
| >Company | >Ingredient | >NDC |
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