Benazepril Hydrochloride
- Product NDC
- 60429-159
- 11-digit product format
- 604290159
- Labeler code
- 60429
- Product ID
- 60429-159_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
- 10 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 |
|---|
| 60429-159-90 | 60429015990 | 90 TABLET, FILM COATED in 1 BOTTLE (60429-159-90) | 2014-07-15 | 0000-00-00 | No | No | Current |