Benazepril Hydrochloride
- Product NDC
- 60760-352
- 11-digit product format
- 607600352
- Labeler code
- 60760
- Product ID
- 60760-352_7a024766-f7af-7685-e053-2a91aa0ab774
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-352 | BENAZEPRIL HYDROCHLORIDE TABLET, COATED [ST. MARY'S MEDICAL PARK PHARMACY] | 3 | Legacy NDC | 20181107_5e9a61dd-9b2e-5b86-e053-2a91aa0a365c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-352-90 | 60760035290 | 90 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-352-90) | 2017-11-15 | 0000-00-00 | No | No | Current |