Benazepril Hydrochloride
- Product NDC
- 43063-748
- 11-digit product format
- 430630748
- Labeler code
- 43063
- Product ID
- 43063-748_51cc6ee4-27b7-62c2-e063-6294a90ada01
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA078212
- Marketing category
- ANDA
- Marketing start
- 2008-05-22
- Marketing end
- 2026-11-30
- Substance
- BENAZEPRIL HYDROCHLORIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Decreased Blood Pressure [PE]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Benazepril Hydrochloride
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENAZEPRIL HYDROCHLORIDE | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | N1SN99T69T |
| Rxcui | 898719 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43063-748-30 | Benazepril Hydrochloride | 30 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 30 | | 30 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43063-748 | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.] | 28 | Current NDC, Legacy NDC, 1 package rows | 20240820_5de2ea54-877d-46e9-b4c2-bf1ab9d0f19c.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 |
|---|
| 43063-748-30 | 43063074830 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-748-30) | 2017-02-24 | 2026-11-30 | No | No | Current |