Benazepril Hydrochloride
- Product NDC
- 50090-0912
- 11-digit product format
- 500900912
- Labeler code
- 50090
- Product ID
- 50090-0912_a6e75821-b27c-4401-a227-9a5bcd280836
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA076820
- Marketing category
- ANDA
- Marketing start
- 2010-02-02
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0912-0 | 50090091200 | 30 TABLET in 1 BOTTLE (50090-0912-0) | 30 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-0912-2 | 50090091202 | 90 TABLET in 1 BOTTLE (50090-0912-2) | 90 tablet | 2010-02-02 | 0000-00-00 | No | No | Current |