NDC 62135-485 – Quinapril
Quinapril Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC62135-485
Product details
- Brand name
- Quinapril
- Generic name
- Quinapril
- Labeler
- Chartwell RX, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076803
- Marketed since
- March 2, 2005
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor
Active ingredients
- Quinapril Hydrochloride 10 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 62135-485-90 | 90 TABLET, FILM COATED in 1 BOTTLE (62135-485-90) | Nov 6, 2023 |
Other Quinapril products
- 65862-620 Quinapril Hydrochloride 40 mg/1 · Tablet, Film Coated · Aurobindo Pharma Limited
- 65862-619 Quinapril Hydrochloride 20 mg/1 · Tablet, Film Coated · Aurobindo Pharma Limited
- 65862-618 Quinapril Hydrochloride 10 mg/1 · Tablet, Film Coated · Aurobindo Pharma Limited
- 65862-617 Quinapril Hydrochloride 5 mg/1 · Tablet, Film Coated · Aurobindo Pharma Limited
- 63629-7934 Quinapril Hydrochloride 10 mg/1 · Tablet, Film Coated · Bryant Ranch Prepack
- 62135-484 Quinapril Hydrochloride 5 mg/1 · Tablet, Film Coated · Chartwell RX, LLC
- 62135-486 Quinapril Hydrochloride 20 mg/1 · Tablet, Film Coated · Chartwell RX, LLC
- 62135-487 Quinapril Hydrochloride 40 mg/1 · Tablet, Film Coated · Chartwell RX, LLC
- 63187-874 Quinapril Hydrochloride 10 mg/1 · Tablet, Film Coated · Proficient Rx LP
- 68001-187 Quinapril Hydrochloride 20 mg/1 · Tablet · BluePoint Laboratories
- 68001-189 Quinapril Hydrochloride 5 mg/1 · Tablet · BluePoint Laboratories
- 68001-188 Quinapril Hydrochloride 10 mg/1 · Tablet · BluePoint Laboratories