Benazepril Hydrochloride
- Product NDC
- 68788-6957
- 11-digit product format
- 687886957
- Labeler code
- 68788
- Product ID
- 68788-6957_5149af12-5ae1-458d-835d-915134a40e2b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076118
- Marketing category
- ANDA
- Marketing start
- 2017-05-02
- 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
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Benazepril Hydrochloride
- Listing expiration
- 2026-12-31
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 |
|---|
| 68788-6957-1 | Benazepril Hydrochloride | 100 in 1 BOTTLE | TABLET, COATED | 100 | | 8 |
| 68788-6957-3 | Benazepril Hydrochloride | 30 in 1 BOTTLE | TABLET, COATED | 30 | | 8 |
| 68788-6957-6 | Benazepril Hydrochloride | 60 in 1 BOTTLE | TABLET, COATED | 60 | | 8 |
| 68788-6957-8 | Benazepril Hydrochloride | 120 in 1 BOTTLE | TABLET, COATED | 120 | | 8 |
| 68788-6957-9 | Benazepril Hydrochloride | 90 in 1 BOTTLE | TABLET, COATED | 90 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-6957 | BENAZEPRIL HYDROCHLORIDE TABLET, COATED [PREFERRED PHARMACEUTICALS INC.] | 8 | Current NDC, Legacy NDC, 5 package rows | 20250126_4d5a8b50-dd2f-4329-9e28-93608e8fe8da.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 |
|---|
| 68788-6957-1 | 68788695701 | 100 TABLET, COATED in 1 BOTTLE (68788-6957-1) | 2017-05-02 | 0000-00-00 | No | No | Current |
| 68788-6957-3 | 68788695703 | 30 TABLET, COATED in 1 BOTTLE (68788-6957-3) | 2017-05-02 | 0000-00-00 | No | No | Current |
| 68788-6957-6 | 68788695706 | 60 TABLET, COATED in 1 BOTTLE (68788-6957-6) | 2017-05-02 | 0000-00-00 | No | No | Current |
| 68788-6957-8 | 68788695708 | 120 TABLET, COATED in 1 BOTTLE (68788-6957-8) | 2017-05-02 | 0000-00-00 | No | No | Current |
| 68788-6957-9 | 68788695709 | 90 TABLET, COATED in 1 BOTTLE (68788-6957-9) | 2017-05-02 | 0000-00-00 | No | No | Current |