NDC 65862-619 – Quinapril
Quinapril Hydrochloride 20 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-619
Product details
- Brand name
- Quinapril
- Generic name
- Quinapril Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202725
- Marketed since
- April 29, 2013
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Quinapril Hydrochloride 20 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 65862-619-19 | 10000 TABLET, FILM COATED in 1 BOTTLE (65862-619-19) | Apr 29, 2013 |
| 65862-619-30 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-619-30) | Apr 29, 2013 |
| 65862-619-78 | 10 BLISTER PACK in 1 CARTON (65862-619-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-619-10) | Apr 29, 2013 |
| 65862-619-90 | 90 TABLET, FILM COATED in 1 BOTTLE (65862-619-90) | Apr 29, 2013 |
| 65862-619-99 | 1000 TABLET, FILM COATED in 1 BOTTLE (65862-619-99) | Apr 29, 2013 |
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