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Losortan Potassium
Losortan Potassium - 68382-136-06 - (Losartan Potassium)
Drug Information of Losortan Potassium
| Product NDC: | 68382-136 |
| Proprietary Name: | Losortan Potassium |
| Non Proprietary Name: | Losartan Potassium |
| Active Ingredient(s): | 50 mg/1 & nbsp; Losartan Potassium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Losortan Potassium
| Product NDC: | 68382-136 |
| Labeler Name: | Zydus Pharmaceuticals (USA) Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078243 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101004 |
Package Information of Losortan Potassium
| Package NDC: | 68382-136-06 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (68382-136-06) |
NDC Information of Losortan Potassium
| NDC Code | 68382-136-06 |
| Proprietary Name | Losortan Potassium |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (68382-136-06) |
| Product NDC | 68382-136 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Losartan Potassium |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20101004 |
| Marketing Category Name | ANDA |
| Labeler Name | Zydus Pharmaceuticals (USA) Inc. |
| Substance Name | LOSARTAN POTASSIUM |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
