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ANTARA
ANTARA - 27437-109-06 - (FENOFIBRATE)
Drug Information of ANTARA
| Product NDC: | 27437-109 |
| Proprietary Name: | ANTARA |
| Non Proprietary Name: | FENOFIBRATE |
| Active Ingredient(s): | 43 mg/1 & nbsp; FENOFIBRATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ANTARA
| Product NDC: | 27437-109 |
| Labeler Name: | LUPIN PHARMA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021695 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090925 |
Package Information of ANTARA
| Package NDC: | 27437-109-06 |
| Package Description: | 30 CAPSULE in 1 BOTTLE (27437-109-06) |
NDC Information of ANTARA
| NDC Code | 27437-109-06 |
| Proprietary Name | ANTARA |
| Package Description | 30 CAPSULE in 1 BOTTLE (27437-109-06) |
| Product NDC | 27437-109 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FENOFIBRATE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20090925 |
| Marketing Category Name | NDA |
| Labeler Name | LUPIN PHARMA |
| Substance Name | FENOFIBRATE |
| Strength Number | 43 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [Chemical/Ingredient] |
