Benazepril Hydrochloride
- Product NDC
- 68071-1969
- 11-digit product format
- 680711969
- Labeler code
- 68071
- Product ID
- 68071-1969_1d605356-58f1-2e0a-e063-6294a90af384
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076118
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- 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
- 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 |
|---|---|
| BENAZEPRIL HYDROCHLORIDE | 20 mg/1 |
Harmonized Identifiers#
| Field | Values |
|---|---|
| Unii | N1SN99T69T |
| Rxcui | 898690 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| a4484670-2869-6416-f6ff-03b1b3cbd1b0 | Product name | 2 | 20190415 |
| 55bffd21-17e1-ff02-2e8f-1f9a532b9502 | Product name | 2 | 20150320 |
| b9fbc696-7d55-c52e-4f12-7e3d99cd2db4 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68071-1969-2 | Benazepril Hydrochloride | 120 in 1 BOTTLE | TABLET, COATED | 120 | 4 | |
| 68071-1969-3 | Benazepril Hydrochloride | 30 in 1 BOTTLE | TABLET, COATED | 30 | 4 | |
| 68071-1969-6 | Benazepril Hydrochloride | 60 in 1 BOTTLE | TABLET, COATED | 60 | 4 | |
| 68071-1969-9 | Benazepril Hydrochloride | 90 in 1 BOTTLE | TABLET, COATED | 90 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68071-1969 | BENAZEPRIL HYDROCHLORIDE TABLET, COATED [NUCARE PHARMACEUTICALS,INC.] | 4 | Current NDC, Legacy NDC, 4 package rows | 20240717_700c828c-86c6-1857-e053-2a91aa0ae314.zip |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 898690 | benazepril HCl 20 MG Oral Tablet | PSN | 700c828c-86c6-1857-e053-2a91aa0ae314 | 4 |
| 898690 | benazepril hydrochloride 20 MG Oral Tablet | SCD | 700c828c-86c6-1857-e053-2a91aa0ae314 | 4 |
| 898690 | BZP hydrochloride 20 MG Oral Tablet | SY | 700c828c-86c6-1857-e053-2a91aa0ae314 | 4 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 68071-1969-2 | 68071196902 | 120 TABLET, COATED in 1 BOTTLE (68071-1969-2) | 2018-07-02 | 0000-00-00 | No | No | Current |
| 68071-1969-3 | 68071196903 | 30 TABLET, COATED in 1 BOTTLE (68071-1969-3) | 2018-07-02 | 0000-00-00 | No | No | Current |
| 68071-1969-6 | 68071196906 | 60 TABLET, COATED in 1 BOTTLE (68071-1969-6) | 2018-07-02 | 0000-00-00 | No | No | Current |
| 68071-1969-9 | 68071196909 | 90 TABLET, COATED in 1 BOTTLE (68071-1969-9) | 2018-07-02 | 0000-00-00 | No | No | Current |