61919-852 : Amoldipine Benazepril Hcl Oral Capsule
| NDC: | 61919-852 |
| Labeler: | Directrx |
| Product Type: | Human Prescription Drug |
| Drug Name: | Amoldipine Benazepril Hcl |
| Dosage Form: | Oral Capsule |
| Application #: | ANDA202239 |
| Rev. Date: |
Appearance:
| Markings: | J;02 |
| Shapes: |
Capsule |
| Colors: |
 Purple |
| Size (mm): | 21 |
| Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. | |
NDC Package Codes:
- 61919-852-90: 90 CAPSULE IN 1 BOTTLE (61919‑852‑90)
Active Ingredients:
- Amlodipine Besylate
- Benazepril Hydrochloride
Dosage Strength:
- 10 mg
- 20 mg
Inactive Ingredients:
- Povidone K30
- Titanium Dioxide
- D&c Red No. 28
- Silicon Dioxide
- Gelatin
- Crospovidone (15 Mpa.s At 5%)
- Magnesium Stearate
- Microcrystalline Cellulose
- Sodium Lauryl Sulfate
- Fd&c Blue No. 1
- Fd&c Red No. 40
- Fd&c Yellow No. 5
- Ferrosoferric Oxide
- Shellac /
Pharmaceutical Classes:
- Angiotensin Converting Enzyme Inhibitor [EPC]
- Angiotensin-converting Enzyme Inhibitors [MoA]
- Calcium Channel Antagonists [MoA]
- Decreased Blood Pressure [PE]
- Dihydropyridine Calcium Channel Blocker [EPC]
- Dihydropyridines [CS]
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.
