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nifedipine
nifedipine - 68084-022-01 - (nifedipine)
Drug Information of nifedipine
| Product NDC: | 68084-022 |
| Proprietary Name: | nifedipine |
| Non Proprietary Name: | nifedipine |
| Active Ingredient(s): | 10 mg/1 & nbsp; nifedipine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of nifedipine
| Product NDC: | 68084-022 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072579 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130624 |
Package Information of nifedipine
| Package NDC: | 68084-022-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (68084-022-01) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (68084-022-11) |
NDC Information of nifedipine
| NDC Code | 68084-022-01 |
| Proprietary Name | nifedipine |
| Package Description | 10 BLISTER PACK in 1 CARTON (68084-022-01) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (68084-022-11) |
| Product NDC | 68084-022 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | nifedipine |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20130624 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | NIFEDIPINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
