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LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE - 68382-142-16 - (LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE)
Drug Information of LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
| Product NDC: | 68382-142 |
| Proprietary Name: | LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE |
| Non Proprietary Name: | LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE |
| Active Ingredient(s): | 12.5; 50 mg/1; mg/1 & nbsp; LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
| Product NDC: | 68382-142 |
| Labeler Name: | Zydus Pharmaceuticals (USA) Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078385 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101004 |
Package Information of LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
| Package NDC: | 68382-142-16 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE (68382-142-16) |
NDC Information of LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
| NDC Code | 68382-142-16 |
| Proprietary Name | LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (68382-142-16) |
| Product NDC | 68382-142 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE |
| 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 | HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM |
| Strength Number | 12.5; 50 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
