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FELODIPINE
FELODIPINE - 64679-414-01 - (FELODIPINE)
Drug Information of FELODIPINE
| Product NDC: | 64679-414 |
| Proprietary Name: | FELODIPINE |
| Non Proprietary Name: | FELODIPINE |
| Active Ingredient(s): | 10 mg/1 & nbsp; FELODIPINE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FELODIPINE
| Product NDC: | 64679-414 |
| Labeler Name: | WOCKHARDT USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091484 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101205 |
Package Information of FELODIPINE
| Package NDC: | 64679-414-01 |
| Package Description: | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-414-01) |
NDC Information of FELODIPINE
| NDC Code | 64679-414-01 |
| Proprietary Name | FELODIPINE |
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-414-01) |
| Product NDC | 64679-414 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FELODIPINE |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20101205 |
| Marketing Category Name | ANDA |
| Labeler Name | WOCKHARDT USA LLC |
| Substance Name | FELODIPINE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
