Benazepril Hydrochloride and Hydrochlorothiazide (Benazepril Hydrochloride and Hydrochlorothiazide) — NDC 68462-579 by Glenmark Ph
Benazepril Hydrochloride and Hydrochlorothiazide (Benazepril Hydrochloride and Hydrochlorothiazide) — NDC 68462-579 by Glenmark Ph is one of 9,000 drug products in the NDCLookup dataset. Key details — Brand name: Benazepril Hydrochloride and Hydrochlorothiazide; Generic name: Benazepril Hydrochloride and Hydrochlorothi
| Brand name | Benazepril Hydrochloride and Hydrochlorothiazide |
|---|---|
| Generic name | Benazepril Hydrochloride and Hydrochlorothiazide |
| Product NDC | 68462-579 |
| Labeler | Glenmark Pharmaceuticals Inc., USA |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Active ingredients | BENAZEPRIL HYDROCHLORIDE 20 mg/1; HYDROCHLOROTHIAZIDE 25 mg/1 |
| Pharmacologic class | Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
| Marketing category | ANDA |
| Product type | HUMAN PRESCRIPTION DRUG |
| Source | openFDA NDC Directory |
$899/mo
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