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Adalat CC
Adalat CC - 50419-701-10 - (nifedipine)
Drug Information of Adalat CC
| Product NDC: | 50419-701 |
| Proprietary Name: | Adalat CC |
| Non Proprietary Name: | nifedipine |
| Active Ingredient(s): | 30 mg/1 & nbsp; nifedipine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Adalat CC
| Product NDC: | 50419-701 |
| Labeler Name: | Bayer HealthCare Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020198 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19930421 |
Package Information of Adalat CC
| Package NDC: | 50419-701-10 |
| Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-701-10) |
NDC Information of Adalat CC
| NDC Code | 50419-701-10 |
| Proprietary Name | Adalat CC |
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-701-10) |
| Product NDC | 50419-701 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nifedipine |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19930421 |
| Marketing Category Name | NDA |
| Labeler Name | Bayer HealthCare Pharmaceuticals Inc. |
| Substance Name | NIFEDIPINE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
