NDC 68151-1472
Moexipril Hydrochloride
Moexipril Hydrochloride
Moexipril Hydrochloride is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Carilion Materials Management. The primary component is Moexipril Hydrochloride.
| Product ID | 68151-1472_2517e55f-cae7-4b4a-8565-7f3569a66ca7 |
| NDC | 68151-1472 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Moexipril Hydrochloride |
| Generic Name | Moexipril Hydrochloride |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2003-05-08 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA076204 |
| Labeler Name | Carilion Materials Management |
| Substance Name | MOEXIPRIL HYDROCHLORIDE |
| Active Ingredient Strength | 8 mg/1 |
| Pharm Classes | Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |