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nifedipine
nifedipine - 59762-6690-8 - (NIFEDIPINE)
Drug Information of nifedipine
| Product NDC: | 59762-6690 |
| Proprietary Name: | nifedipine |
| Non Proprietary Name: | NIFEDIPINE |
| Active Ingredient(s): | 30 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 nifedipine
| Product NDC: | 59762-6690 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019684 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20100331 |
Package Information of nifedipine
| Package NDC: | 59762-6690-8 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (59762-6690-8) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of nifedipine
| NDC Code | 59762-6690-8 |
| Proprietary Name | nifedipine |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (59762-6690-8) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 59762-6690 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | NIFEDIPINE |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100331 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Greenstone LLC |
| Substance Name | NIFEDIPINE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
