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Nifediac CC
Nifediac CC - 53808-0500-1 - (Nifedipine)
Drug Information of Nifediac CC
| Product NDC: | 53808-0500 |
| Proprietary Name: | Nifediac CC |
| Non Proprietary Name: | Nifedipine |
| Active Ingredient(s): | 90 mg/1 & nbsp; Nifedipine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nifediac CC
| Product NDC: | 53808-0500 |
| Labeler Name: | State of Florida DOH Central Pharmacy |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076070 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090701 |
Package Information of Nifediac CC
| Package NDC: | 53808-0500-1 |
| Package Description: | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (53808-0500-1) |
NDC Information of Nifediac CC
| NDC Code | 53808-0500-1 |
| Proprietary Name | Nifediac CC |
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (53808-0500-1) |
| Product NDC | 53808-0500 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nifedipine |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20090701 |
| Marketing Category Name | ANDA |
| Labeler Name | State of Florida DOH Central Pharmacy |
| Substance Name | NIFEDIPINE |
| Strength Number | 90 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
