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USFDA APPLICATION NUMBER - 18482 / DOSAGE - CAPSULE;ORAL - 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| NIFEDIPINE(UNII: I9ZF7L6G2L) (NIFEDIPINE - UNII:I9ZF7L6G2L) | NIFEDIPINE | 10mg |
Inactive Ingredients
| Ingredient Name | Pfizer Laboratories Div Pfizer Inc | REMEDYREPACK INC. |
|---|---|---|
| FD&C YELLOW NO. 6(H77VEI93A8) | ||
| FERRIC OXIDE RED(1K09F3G675) | ||
| GLYCERIN(PDC6A3C0OX) | ||
| PEPPERMINT OIL(AV092KU4JH) | ||
| POLYETHYLENE GLYCOL, UNSPECIFIED(3WJQ0SDW1A) | ||
| POLYETHYLENE GLYCOLS(3WJQ0SDW1A) | ||
| SACCHARIN SODIUM ANHYDROUS(I4807BK602) | ||
| SACCHARIN SODIUM(SB8ZUX40TY) | ||
| WATER BUFFALO, COOKED(RM3G76I0A1) | ||
| WATER(059QF0KO0R) |
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