NDC 68180-758 – Amlodipine Besylate and Benazepril Hydrochloride
Amlodipine Besylate 10 mg/1; Benazepril Hydrochloride 20 mg/1 · Capsule · Oral
Product NDC68180-758
Product details
- Brand name
- Amlodipine Besylate and Benazepril Hydrochloride
- Generic name
- Amlodipine Besylate and Benazepril Hydrochloride
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Capsule
- Route
- Oral
- Marketing category
- ANDA · ANDA078466
- Marketed since
- February 5, 2010
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin Converting Enzyme Inhibitor; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker
Active ingredients
- Amlodipine Besylate 10 mg/1
- Benazepril Hydrochloride 20 mg/1
Uses, dosage, side effects and warnings for Amlodipine Besylate and Benazepril Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68180-758-01 | 100 CAPSULE in 1 BOTTLE (68180-758-01) | Feb 5, 2010 |
| 68180-758-02 | 500 CAPSULE in 1 BOTTLE (68180-758-02) | Feb 5, 2010 |
Recalls mentioning this NDC
- D-0542-2025 Aug 6, 2025 · Class II
Labeling: Incorrect or Missing Lot and/or Exp Date: released with wrong expiry date as Feb.2027 instead of Jan.2027
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