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losartan potassium and hydrochlorothiazide
losartan potassium and hydrochlorothiazide - 0781-5818-31 - (losartan potassium and hydrochlorothiazide)
Drug Information of losartan potassium and hydrochlorothiazide
| Product NDC: | 0781-5818 |
| Proprietary Name: | losartan potassium and hydrochlorothiazide |
| Non Proprietary Name: | losartan potassium and hydrochlorothiazide |
| Active Ingredient(s): | 25; 100 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: | 0781-5818 |
| Labeler Name: | Sandoz Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020387 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19950428 |
Package Information of losartan potassium and hydrochlorothiazide
| Package NDC: | 0781-5818-31 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (0781-5818-31) |
NDC Information of losartan potassium and hydrochlorothiazide
| NDC Code | 0781-5818-31 |
| Proprietary Name | losartan potassium and hydrochlorothiazide |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0781-5818-31) |
| Product NDC | 0781-5818 |
| 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 | 19950428 |
| Marketing Category Name | NDA |
| Labeler Name | Sandoz Inc. |
| Substance Name | HYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM |
| Strength Number | 25; 100 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
