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FELODIPINE
FELODIPINE - 55648-412-02 - (FELODIPINE)
Drug Information of FELODIPINE
| Product NDC: | 55648-412 |
| Proprietary Name: | FELODIPINE |
| Non Proprietary Name: | FELODIPINE |
| Active Ingredient(s): | 5 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: | 55648-412 |
| Labeler Name: | WOCKHARDT LIMITED |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091484 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101205 |
Package Information of FELODIPINE
| Package NDC: | 55648-412-02 |
| Package Description: | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-412-02) |
NDC Information of FELODIPINE
| NDC Code | 55648-412-02 |
| Proprietary Name | FELODIPINE |
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-412-02) |
| Product NDC | 55648-412 |
| 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 LIMITED |
| Substance Name | FELODIPINE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
