Benazepril
- Product NDC
- 61919-739
- 11-digit product format
- 619190739
- Labeler code
- 61919
- Product ID
- 61919-739_cc7107fc-0dd8-f2fd-e053-2a95a90a5011
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA076118
- Marketing category
- ANDA
- Marketing start
- 2019-01-15
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-739-90 | Benazepril | 90 in 1 BOTTLE | TABLET, COATED | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-739 | BENAZEPRIL TABLET, COATED BENAZEPRIL HYDROCHLORIDE TABLET, COATED [DIRECT_RX] | 2 | Legacy NDC, 1 package rows | 20210921_7f819b77-2600-0a5f-e053-2a91aa0a9d15.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-739-90 | 61919073990 | 90 TABLET, COATED in 1 BOTTLE (61919-739-90) | 2019-01-15 | 0000-00-00 | No | No | Current |