United States · FDA National Drug Code directory
Quinapril
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 65862-619_5263abd5-ce46-4918-9bb0-9632861bcbc9
- Product NDC
- 65862-619
- Form
- TABLET, FILM COATED
- Composition / generic term
- Quinapril Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20130429
- Source listing expiry
- 20261231
Source-listed ingredients
- QUINAPRIL HYDROCHLORIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10000 TABLET, FILM COATED in 1 BOTTLE (65862-619-19) · 65862-619-19
- 30 TABLET, FILM COATED in 1 BOTTLE (65862-619-30) · 65862-619-30
- 10 BLISTER PACK in 1 CARTON (65862-619-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-619-10) · 65862-619-78
- 90 TABLET, FILM COATED in 1 BOTTLE (65862-619-90) · 65862-619-90
- 1000 TABLET, FILM COATED in 1 BOTTLE (65862-619-99) · 65862-619-99
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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