Moexipril Hydrochloride and Hydrochlorothiazide is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Avkare, Inc.. The primary component is Moexipril Hydrochloride; Hydrochlorothiazide.
| Product ID | 42291-576_63b63711-ed6d-be1f-e053-2991aa0a0390 | 
| NDC | 42291-576 | 
| 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 | 2017-04-03 | 
| Marketing Category | ANDA / ANDA | 
| Application Number | ANDA076980 | 
| Labeler Name | AvKARE, Inc. | 
| 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 | 2017-04-03 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | ANDA | 
| Application Number | ANDA076980 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2017-04-03 | 
| Marketing End Date | 2020-02-03 | 
| Ingredient | Strength | 
|---|---|
| MOEXIPRIL HYDROCHLORIDE | 7.5 mg/1 | 
| SPL SET ID: | a78ce872-b230-48cf-a91d-92667d643386 | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code | 
| 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 |