NDC 65862-161 – Quinapril Hydrochloride/hydrochlorothiazide
Quinapril Hydrochloride 10 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-161
Product details
- Brand name
- Quinapril Hydrochloride/hydrochlorothiazide
- Generic name
- Quinapril Hydrochloride/hydrochlorothiazide
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078450
- Marketed since
- August 24, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic
Active ingredients
- Quinapril Hydrochloride 10 mg/1
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Quinapril Hydrochloride/hydrochlorothiazide →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 65862-161-90 | 90 TABLET, FILM COATED in 1 BOTTLE (65862-161-90) | Aug 24, 2007 |
Recalls mentioning this NDC
- D-0021-2023 Nov 2, 2022 · Class II
CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.