Benazepril Hydrochloride
- Product NDC
- 53217-190
- 11-digit product format
- 532170190
- Labeler code
- 53217
- Product ID
- 53217-190_8b5b8721-2499-4599-a23b-5d16dae55e09
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Benazepril Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA076118
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- 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 |
|---|
| 53217-190-30 | Benazepril Hydrochloride | 30 in 1 BOTTLE | TABLET, COATED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53217-190 | BENAZEPRIL HYDROCHLORIDE TABLET, COATED [AIDAREX PHARMACEUTICALS LLC] | 1 | Legacy NDC, 1 package rows | 20170302_ce4add14-717c-47f9-b9c4-bdc58d585e5e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-190-30 | 53217019030 | 30 in 1 BOTTLE | Historical |