Benazepril Hydrochloride
- Product NDC
- 55700-291
- 11-digit product format
- 557000291
- Labeler code
- 55700
- Product ID
- 55700-291_562745d4-2d66-400a-a461-b97d761aa052
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA076118
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-291-30 | 55700029130 | 30 TABLET, COATED in 1 BOTTLE (55700-291-30) | 2015-09-03 | 0000-00-00 | No | No | Current |
| 55700-291-90 | 55700029190 | 90 TABLET, COATED in 1 BOTTLE (55700-291-90) | 2015-09-03 | 0000-00-00 | No | No | Current |