Moexipril Hydrochloride and Hydrochlorothiazide - Moexipril Hydrochloride and Hydrochlorothiazide
Navigation: NDC > Supplier starting with: G > GLENMARK GENERICS INC., USA| Field | Value |
|---|---|
| NDC Code: | 68462-207 |
| Proprietary Name: | Moexipril Hydrochloride and Hydrochlorothiazide |
| Suffix: | |
| Non-Proprietary Name: | Moexipril Hydrochloride and Hydrochlorothiazide |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 18-03-2010 |
| Category Name: | ANDA |
| Application Number: | ANDA090718 |
| Labeler: | GLENMARK GENERICS INC., USA |
| Substance Name: | HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE |
| Active Numerator Strength: | 12.5; 7.5 |
| Active Ingredient Unit: | mg/1; mg/1 |
| Pharm Classes: | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
| DEA Schedule: |