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Procardia
Procardia - 52125-126-02 - (NIFEDIPINE)
Drug Information of Procardia
| Product NDC: | 52125-126 |
| Proprietary Name: | Procardia |
| Non Proprietary Name: | NIFEDIPINE |
| Active Ingredient(s): | 10 mg/1 & nbsp; NIFEDIPINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Procardia
| Product NDC: | 52125-126 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018482 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130225 |
Package Information of Procardia
| Package NDC: | 52125-126-02 |
| Package Description: | 30 CAPSULE in 1 BLISTER PACK (52125-126-02) |
NDC Information of Procardia
| NDC Code | 52125-126-02 |
| Proprietary Name | Procardia |
| Package Description | 30 CAPSULE in 1 BLISTER PACK (52125-126-02) |
| Product NDC | 52125-126 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | NIFEDIPINE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20130225 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | NIFEDIPINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
