Benazepril hydrochloride
- Product NDC
- 62135-720
- 11-digit product format
- 621350720
- Labeler code
- 62135
- Product ID
- 62135-720_24246e61-c66b-9c3e-e063-6294a90a5207
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA076267
- Marketing category
- ANDA
- Marketing start
- 2022-08-20
- 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
- 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 | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | N1SN99T69T |
| Rxcui | 898687, 898690, 898719, 898723 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62135-720-90 | Benazepril hydrochloride | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-720 | BENAZEPRIL HYDROCHLORIDE TABLET [CHARTWELL RX, LLC] | 2 | Current NDC, 1 package rows | 20241012_df13d8d8-0d70-4d6f-9dd1-5da38fbe2562.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 62135-720-90 | 62135072090 | 90 TABLET in 1 BOTTLE (62135-720-90) | 90 tablet | 2023-07-20 | No | No | Current |