Benazepril Hydrochloride
- Product NDC
- 21695-612
- 11-digit product format
- 216950612
- Labeler code
- 21695
- Product ID
- 21695-612_56ffd662-60a6-4b43-a7ea-f778714dfbbd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rebel Distributors Corp.
- Application
- ANDA076402
- Marketing category
- ANDA
- Marketing start
- 2004-02-11
- Marketing end
- 0000-00-00
- Substance
- BENAZEPRIL HYDROCHLORIDE
- Active strength
- 5 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 |
|---|
| 21695-612-90 | Benazepril Hydrochloride | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 1 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| benazepril hydrochloride | ACTIVE INGREDIENT | N1SN99T69T | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | |
| D&C YELLOW NO. 10 | ACTIVE INGREDIENT | 35SW5USQ3G | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | |
| benazepril | ACTIVE MOIETY | UDM7Q7QWP8 | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | |
| colloidal silicon dioxide | INACTIVE INGREDIENT | ETJ7Z6XBU4 | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | |
| crospovidone | INACTIVE INGREDIENT | 68401960MK | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | |
| D&C YELLOW NO. 10 | INACTIVE INGREDIENT | 35SW5USQ3G | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | |
| FD&C RED NO. 40 | INACTIVE INGREDIENT | WZB9127XOA | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | |
| FD&C YELLOW NO. 6 | INACTIVE INGREDIENT | H77VEI93A8 | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | |
| HYDROGENATED CASTOR OIL | INACTIVE INGREDIENT | ZF94AP8MEY | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | |
| hypromellose | INACTIVE INGREDIENT | 3NXW29V3WO | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | |
| lactose monohydrate | INACTIVE INGREDIENT | EWQ57Q8I5X | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | |
| polyethylene glycol | INACTIVE INGREDIENT | 3WJQ0SDW1A | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | |
| POLYSORBATE 20 | INACTIVE INGREDIENT | 7T1F30V5YH | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | |
| titanium dioxide | INACTIVE INGREDIENT | 15FIX9V2JP | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | |
| zinc stearate | INACTIVE INGREDIENT | H92E6QA4FV | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-612 | BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP.] | 1 | Legacy NDC, 1 package rows | 20100921_56ffd662-60a6-4b43-a7ea-f778714dfbbd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-612-90 | 21695061290 | 90 in 1 BOTTLE | Historical |