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AFEDITAB
AFEDITAB - 49349-000-02 - (NIFEDIPINE)
Drug Information of AFEDITAB
| Product NDC: | 49349-000 |
| Proprietary Name: | AFEDITAB |
| Non Proprietary Name: | NIFEDIPINE |
| Active Ingredient(s): | 60 mg/60mg & nbsp; NIFEDIPINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AFEDITAB
| Product NDC: | 49349-000 |
| Labeler Name: | RemedyRepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA123456 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100513 |
Package Information of AFEDITAB
| Package NDC: | 49349-000-02 |
| Package Description: | 30 mg in 1 BLISTER PACK (49349-000-02) |
NDC Information of AFEDITAB
| NDC Code | 49349-000-02 |
| Proprietary Name | AFEDITAB |
| Package Description | 30 mg in 1 BLISTER PACK (49349-000-02) |
| Product NDC | 49349-000 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | NIFEDIPINE |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100513 |
| Marketing Category Name | NDA |
| Labeler Name | RemedyRepack |
| Substance Name | NIFEDIPINE |
| Strength Number | 60 |
| Strength Unit | mg/60mg |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
