Amlodipine and Benazepril Hydrochloride
- Product NDC
- 84677-013
- 11-digit product format
- 846770013
- Labeler code
- 84677
- Product ID
- 84677-013_4b35268c-9ae9-b3e8-e063-6394a90a9a86
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amlodipine and Benazepril Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA091431
- Marketing category
- ANDA
- Marketing start
- 2013-12-30
- Substance
- AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
- Active strength
- 10; 40 mg/1; mg/1
- Pharmacologic classes
- Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Decreased Blood Pressure [PE], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Amlodipine and Benazepril Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AMLODIPINE BESYLATE | 10 mg/1 |
| BENAZEPRIL HYDROCHLORIDE | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 864V2Q084H, N1SN99T69T |
| Rxcui | 898346 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84677-013-01 | Amlodipine and Benazepril Hydrochloride | 100 in 1 BOTTLE | CAPSULE | 100 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84677-013-01 | 84677001301 | 100 CAPSULE in 1 BOTTLE (84677-013-01) | 100 capsule | 2025-10-28 | No | No | Current |