| NDC Code | 0069-2660-72 |
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| Package Description | 300 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-2660-72) |
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| Product NDC | 0069-2660 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Procardia |
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| Proprietary Name Suffix | Xl |
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| Non-Proprietary Name | Nifedipine |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 19890906 |
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| Marketing Category Name | NDA |
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| Application Number | NDA019684 |
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| Manufacturer | Pfizer Laboratories Div Pfizer Inc |
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| Substance Name | NIFEDIPINE |
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| Strength | 60 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |
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