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Losartan Potassium
Losartan Potassium - 51079-750-20 - (losartan potassium)
Drug Information of Losartan Potassium
| Product NDC: | 51079-750 |
| Proprietary Name: | Losartan Potassium |
| Non Proprietary Name: | losartan potassium |
| Active Ingredient(s): | 25 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: | 51079-750 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091590 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110812 |
Package Information of Losartan Potassium
| Package NDC: | 51079-750-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-750-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-750-01) |
NDC Information of Losartan Potassium
| NDC Code | 51079-750-20 |
| Proprietary Name | Losartan Potassium |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-750-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-750-01) |
| Product NDC | 51079-750 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | losartan potassium |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110812 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | LOSARTAN POTASSIUM |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
