Benazepril Hydrochloride
- Product NDC
- 70518-3074
- 11-digit product format
- 705183074
- Labeler code
- 70518
- Product ID
- 70518-3074_c059a523-a21e-849b-e053-2995a90a4289
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA078212
- Marketing category
- ANDA
- Marketing start
- 2021-04-19
- 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
- 2022-12-31
- 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 |
|---|
| 70518-3074-0 | 70518307400 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3074-0) | 2021-04-19 | 0000-00-00 | No | No | Current |