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Moexipril Hydrochloride and Hydrochlorothiazide
Moexipril Hydrochloride and Hydrochlorothiazide - 68462-207-10 - (Moexipril Hydrochloride and Hydrochlorothiazide)
Drug Information of Moexipril Hydrochloride and Hydrochlorothiazide
| Product NDC: | 68462-207 |
| Proprietary Name: | Moexipril Hydrochloride and Hydrochlorothiazide |
| Non Proprietary Name: | Moexipril Hydrochloride and Hydrochlorothiazide |
| Active Ingredient(s): | 12.5; 7.5 mg/1; mg/1 & nbsp; Moexipril Hydrochloride and Hydrochlorothiazide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Moexipril Hydrochloride and Hydrochlorothiazide
| Product NDC: | 68462-207 |
| Labeler Name: | Glenmark Generics Inc., USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090718 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100318 |
Package Information of Moexipril Hydrochloride and Hydrochlorothiazide
| Package NDC: | 68462-207-10 |
| Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE (68462-207-10) |
NDC Information of Moexipril Hydrochloride and Hydrochlorothiazide
| NDC Code | 68462-207-10 |
| Proprietary Name | Moexipril Hydrochloride and Hydrochlorothiazide |
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (68462-207-10) |
| Product NDC | 68462-207 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Moexipril Hydrochloride and Hydrochlorothiazide |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20100318 |
| Marketing Category Name | ANDA |
| Labeler Name | Glenmark Generics Inc., USA |
| Substance Name | HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE |
| Strength Number | 12.5; 7.5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
