NDC 68382-122 – Amlodipine Besylate
Amlodipine Besylate 5 mg/1 · Tablet · Oral
Product NDC68382-122
Product details
- Brand name
- Amlodipine Besylate
- Generic name
- Amlodipine Besylate
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078226
- Marketed since
- September 21, 2007
- Listing expires
- December 31, 2026
- Pharmacologic class
- Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker
Active ingredients
- Amlodipine Besylate 5 mg/1
Uses, dosage, side effects and warnings for Amlodipine besylate →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 68382-122-01 | 100 TABLET in 1 BOTTLE (68382-122-01) | Sep 21, 2007 |
| 68382-122-05 | 500 TABLET in 1 BOTTLE (68382-122-05) | Sep 21, 2007 |
| 68382-122-16 | 90 TABLET in 1 BOTTLE (68382-122-16) | Sep 21, 2007 |
| 68382-122-77 | 10 BLISTER PACK in 1 CARTON (68382-122-77) / 10 TABLET in 1 BLISTER PACK | Sep 21, 2007 |
Recalls mentioning this NDC
- D-0257-2015 Dec 3, 2014 · Class III
Discoloration: Brown spots were noted embedded in Amlodipine Besylate Tablets, 10 mg, Lot # MP4344.
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