Benazepril Hydrochloride
- Product NDC
- 60429-160
- 11-digit product format
- 604290160
- Labeler code
- 60429
- Product ID
- 60429-160_9273bf56-2787-0971-e053-2995a90ac683
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA076402
- Marketing category
- ANDA
- Marketing start
- 2004-02-11
- Marketing end
- 0000-00-00
- Substance
- BENAZEPRIL HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60429-160-01 | 60429016001 | 100 TABLET, FILM COATED in 1 BOTTLE (60429-160-01) | 2014-07-15 | 0000-00-00 | No | No | Current |
| 60429-160-05 | 60429016005 | 500 TABLET, FILM COATED in 1 BOTTLE (60429-160-05) | 2014-07-15 | 0000-00-00 | No | No | Current |
| 60429-160-18 | 60429016018 | 180 TABLET, FILM COATED in 1 BOTTLE (60429-160-18) | 2014-07-15 | 0000-00-00 | No | No | Current |
| 60429-160-90 | 60429016090 | 90 TABLET, FILM COATED in 1 BOTTLE (60429-160-90) | 2014-07-15 | 0000-00-00 | No | No | Current |