NDC 69097-842 – Quinapril
Quinapril Hydrochloride 20 mg/1 · Tablet · Oral
Product NDC69097-842
Product details
- Brand name
- Quinapril
- Generic name
- Quinapril
- Labeler
- Cipla USA Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078457
- Marketed since
- July 22, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Quinapril Hydrochloride 20 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 69097-842-05 | 90 TABLET in 1 BOTTLE (69097-842-05) | Jul 22, 2016 |
| 69097-842-15 | 1000 TABLET in 1 BOTTLE (69097-842-15) | Jul 22, 2016 |
Other Quinapril products
- 68001-187 Quinapril Hydrochloride 20 mg/1 · Tablet · BluePoint Laboratories
- 68001-189 Quinapril Hydrochloride 5 mg/1 · Tablet · BluePoint Laboratories
- 68001-260 Quinapril Hydrochloride 40 mg/1 · Tablet · BluePoint Laboratories
- 68001-188 Quinapril Hydrochloride 10 mg/1 · Tablet · BluePoint Laboratories
- 71335-1134 Quinapril Hydrochloride 10 mg/1 · Tablet · Bryant Ranch Prepack
- 71335-1707 Quinapril Hydrochloride 10 mg/1 · Tablet · Bryant Ranch Prepack
- 63629-8710 Quinapril Hydrochloride 20 mg/1 · Tablet · Bryant Ranch Prepack
- 69097-839 Quinapril Hydrochloride 5 mg/1 · Tablet · Cipla USA Inc.
- 69097-841 Quinapril Hydrochloride 10 mg/1 · Tablet · Cipla USA Inc.
- 69097-843 Quinapril Hydrochloride 40 mg/1 · Tablet · Cipla USA Inc.
- 68180-558 Quinapril Hydrochloride 20 mg/1 · Tablet · Lupin Pharmaceuticals, Inc.
- 68180-559 Quinapril Hydrochloride 40 mg/1 · Tablet · Lupin Pharmaceuticals, Inc.