NDC 70518-1928 – Amlodipine and Benazepril Hydrochloride
Amlodipine Besylate 5 mg/1; Benazepril Hydrochloride 10 mg/1 · Capsule · Oral
Product NDC70518-1928
Product details
- Brand name
- Amlodipine and Benazepril Hydrochloride
- Generic name
- Amlodipine and Benazepril Hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA202239
- Marketed since
- March 1, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker
Active ingredients
- Amlodipine Besylate 5 mg/1
- Benazepril Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Amlodipine and Benazepril Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70518-1928-0 | 90 CAPSULE in 1 BOTTLE, PLASTIC (70518-1928-0) | Mar 1, 2019 |
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