BENAZEPRIL HYDROCHLORIDE
- Product NDC
- 61919-280
- 11-digit product format
- 619190280
- Labeler code
- 61919
- Product ID
- 61919-280_9c5941d2-5a11-a016-e053-2a95a90a4fea
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BENAZEPRIL HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA076820
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- 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
- 2021-12-31
- 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 |
|---|
| 61919-280-30 | BENAZEPRIL HYDROCHLORIDE | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-280 | BENAZEPRIL HYDROCHLORIDE TABLET [DIRECT RX] | 3 | Legacy NDC, 1 package rows | 20200130_06f1a636-2306-4bbb-9573-cf461adda04c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-280-30 | 61919028030 | 30 TABLET in 1 BOTTLE (61919-280-30) | 30 tablet | 2014-01-01 | 0000-00-00 | No | No | Current |