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Losartan potassium
Losartan potassium - 33342-046-07 - (Losartan potassium)
Drug Information of Losartan potassium
| Product NDC: | 33342-046 |
| Proprietary Name: | Losartan potassium |
| Non Proprietary Name: | Losartan potassium |
| Active Ingredient(s): | 100 mg/1 & nbsp; Losartan potassium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Losartan potassium
| Product NDC: | 33342-046 |
| Labeler Name: | Macleods Pharmaceuticals Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202230 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120601 |
Package Information of Losartan potassium
| Package NDC: | 33342-046-07 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (33342-046-07) |
NDC Information of Losartan potassium
| NDC Code | 33342-046-07 |
| Proprietary Name | Losartan potassium |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (33342-046-07) |
| Product NDC | 33342-046 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Losartan potassium |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120601 |
| Marketing Category Name | ANDA |
| Labeler Name | Macleods Pharmaceuticals Limited |
| Substance Name | LOSARTAN POTASSIUM |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
