Moexipril Hydrochloride and Hydrochlorothiazide is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Glenmark Pharmaceuticals Inc., Usa. The primary component is Moexipril Hydrochloride; Hydrochlorothiazide.
| Product ID | 68462-207_45df7b71-b418-4b22-a0a5-d12916b7b53f |
| NDC | 68462-207 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Moexipril Hydrochloride and Hydrochlorothiazide |
| Generic Name | Moexipril Hydrochloride And Hydrochlorothiazide |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2010-03-18 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA090718 |
| Labeler Name | Glenmark Pharmaceuticals Inc., USA |
| Substance Name | MOEXIPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
| Active Ingredient Strength | 8 mg/1; mg/1 |
| Pharm Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2010-03-18 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA090718 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-03-18 |
| Marketing End Date | 2019-09-11 |
| Marketing Category | ANDA |
| Application Number | ANDA090718 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-03-18 |
| Marketing End Date | 2019-09-11 |
| Marketing Category | ANDA |
| Application Number | ANDA090718 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-03-18 |
| Marketing End Date | 2019-09-11 |
| Ingredient | Strength |
|---|---|
| MOEXIPRIL HYDROCHLORIDE | 7.5 mg/1 |
| SPL SET ID: | e71002c8-3463-4950-b984-c4eee356a5f2 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0093-5213 | Moexipril Hydrochloride and Hydrochlorothiazide | Moexipril Hydrochloride and Hydrochlorothiazide |
| 0093-5214 | Moexipril Hydrochloride and Hydrochlorothiazide | Moexipril Hydrochloride and Hydrochlorothiazide |
| 0093-5215 | Moexipril Hydrochloride and Hydrochlorothiazide | Moexipril Hydrochloride and Hydrochlorothiazide |
| 23155-035 | Moexipril hydrochloride and hydrochlorothiazide | Moexipril hydrochloride and hydrochlorothiazide |
| 23155-036 | Moexipril hydrochloride and hydrochlorothiazide | Moexipril hydrochloride and hydrochlorothiazide |
| 23155-037 | Moexipril hydrochloride and hydrochlorothiazide | Moexipril hydrochloride and hydrochlorothiazide |
| 42291-576 | Moexipril Hydrochloride and Hydrochlorothiazide | Moexipril Hydrochloride and Hydrochlorothiazide |
| 42291-577 | Moexipril Hydrochloride and Hydrochlorothiazide | Moexipril Hydrochloride and Hydrochlorothiazide |
| 42291-578 | Moexipril Hydrochloride and Hydrochlorothiazide | Moexipril Hydrochloride and Hydrochlorothiazide |
| 68462-205 | Moexipril Hydrochloride and Hydrochlorothiazide | Moexipril Hydrochloride and Hydrochlorothiazide |
| 68462-206 | Moexipril Hydrochloride and Hydrochlorothiazide | Moexipril Hydrochloride and Hydrochlorothiazide |
| 68462-207 | Moexipril Hydrochloride and Hydrochlorothiazide | Moexipril Hydrochloride and Hydrochlorothiazide |