NDC 68180-557 – Quinapril
Quinapril Hydrochloride 10 mg/1 · Tablet · Oral
Product NDC68180-557
Product details
- Brand name
- Quinapril
- Generic name
- Quinapril
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA077690
- Marketed since
- February 26, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Quinapril Hydrochloride 10 mg/1
Package NDC codes (0)
| Package NDC | Description | Since |
|---|
Recalls mentioning this NDC
- D-0089-2023 Dec 28, 2022 · Class II
CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit. - D-0088-2023 Dec 28, 2022 · Class II
CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit. - D-0650-2017 Apr 12, 2017 · Class III
Failed Impurities/Degradation Specifications; Impurity A - D-409-2014 Jan 22, 2014 · Class II
Failed Impurities/Degradation Specifications: During stability testing an unknown impurity was found to be above the specification limit at 36 month test interval - D-408-2014 Jan 22, 2014 · Class II
Failed Impurities/Degradation Specifications: During stability testing an unknown impurity was found to be above the specification limit at 36 month test interval
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- 68180-559 Quinapril Hydrochloride 40 mg/1 · Tablet · Lupin Pharmaceuticals, Inc.