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Valsartan and Hydrochlorothiazide
Valsartan and Hydrochlorothiazide - 68180-102-11 - (Valsartan and Hydrochlorothiazide)
Drug Information of Valsartan and Hydrochlorothiazide
| Product NDC: | 68180-102 |
| Proprietary Name: | Valsartan and Hydrochlorothiazide |
| Non Proprietary Name: | Valsartan and Hydrochlorothiazide |
| Active Ingredient(s): | 25; 320 mg/1; mg/1 & nbsp; Valsartan and Hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Valsartan and Hydrochlorothiazide
| Product NDC: | 68180-102 |
| Labeler Name: | Lupin Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078946 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130321 |
Package Information of Valsartan and Hydrochlorothiazide
| Package NDC: | 68180-102-11 |
| Package Description: | 10 TABLET, FILM COATED in 1 BLISTER PACK (68180-102-11) |
NDC Information of Valsartan and Hydrochlorothiazide
| NDC Code | 68180-102-11 |
| Proprietary Name | Valsartan and Hydrochlorothiazide |
| Package Description | 10 TABLET, FILM COATED in 1 BLISTER PACK (68180-102-11) |
| Product NDC | 68180-102 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Valsartan and Hydrochlorothiazide |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130321 |
| Marketing Category Name | ANDA |
| Labeler Name | Lupin Pharmaceuticals, Inc. |
| Substance Name | HYDROCHLOROTHIAZIDE; VALSARTAN |
| Strength Number | 25; 320 |
| 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] |
