NDC 55111-339 – Amlodipine Besylate and Benazepril Hydrochloride
Amlodipine Besylate 5 mg/1; Benazepril Hydrochloride 10 mg/1 · Capsule · Oral
Product NDC55111-339
Product details
- Brand name
- Amlodipine Besylate and Benazepril Hydrochloride
- Generic name
- Amlodipine Besylate and Benazepril Hydrochloride
- Labeler
- Dr.Reddy's Laboratories Limited
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA077183
- Marketed since
- April 19, 2010
- Listing expires
- December 31, 2026
- 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 Besylate and Benazepril Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 55111-339-01 | 100 CAPSULE in 1 BOTTLE (55111-339-01) | Apr 19, 2010 |
| 55111-339-05 | 500 CAPSULE in 1 BOTTLE (55111-339-05) | Apr 19, 2010 |
| 55111-339-30 | 30 CAPSULE in 1 BOTTLE (55111-339-30) | Apr 19, 2010 |
Recalls mentioning this NDC
- D-1434-2012 Aug 8, 2012 · Class II
Adulterated Presence of Foreign Tablets: Dr. Reddy's Laboratories has received complaints of mislabeled bottles of Amlodipine Besylate and Benazepril Hydrochloride Capsules and Ciprofloxacin Tablets.
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