NDC 67877-197 – Amlodipine Besylate
Amlodipine Besylate 2.5 mg/1 · Tablet · Oral
Product NDC67877-197
Product details
- Brand name
- Amlodipine Besylate
- Generic name
- Amlodipine besylate
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA078925
- Marketed since
- October 20, 2010
- Listing expires
- December 31, 2026
- Pharmacologic class
- Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker
Active ingredients
- Amlodipine Besylate 2.5 mg/1
Uses, dosage, side effects and warnings for Amlodipine besylate →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 67877-197-05 | 500 TABLET in 1 BOTTLE (67877-197-05) | Oct 20, 2010 |
| 67877-197-10 | 1000 TABLET in 1 BOTTLE (67877-197-10) | Oct 20, 2010 |
| 67877-197-38 | 10 BLISTER PACK in 1 CARTON (67877-197-38) / 10 TABLET in 1 BLISTER PACK | Oct 20, 2010 |
| 67877-197-90 | 90 TABLET in 1 BOTTLE (67877-197-90) | Oct 20, 2010 |
Recalls mentioning this NDC
- D-1134-2017 Sep 20, 2017 · Class III
PRESENCE OF FOREIGN TABLETS/CAPSULES: A 2.5 mg Amlodipine Besylate tablet was found co-mingled with 10 mg Amlodipine Besylate tablets in a bottle labeled as Amlodipine Besylate 10 mg.
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