Benazepril Hydrochloride
- Product NDC
- 10544-554
- 11-digit product format
- 105440554
- Labeler code
- 10544
- Product ID
- 10544-554_0f553cbe-ba72-283e-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Blenheim Pharmacal, Inc.
- Application
- ANDA076820
- Marketing category
- ANDA
- Marketing start
- 2013-11-08
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 10544-554-30 | Benazepril Hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 10544-554-90 | Benazepril Hydrochloride | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10544-554 | BENAZEPRIL HYDROCHLORIDE TABLET [BLENHEIM PHARMACAL, INC.] | 1 | Legacy NDC, 2 package rows | 20150218_0f553cbe-ba71-283e-e054-00144ff88e88.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10544-554-30 | 10544055430 | 30 in 1 BOTTLE | Historical |
| 10544-554-90 | 10544055490 | 90 in 1 BOTTLE | Historical |