NDC 65862-854 – Amlodipine and Olmesartan Medoxomil
Amlodipine Besylate 5 mg/1; Olmesartan Medoxomil 20 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-854
Product details
- Brand name
- Amlodipine and Olmesartan Medoxomil
- Generic name
- Amlodipine and Olmesartan Medoxomil
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA206906
- Marketed since
- May 15, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker
Active ingredients
- Amlodipine Besylate 5 mg/1
- Olmesartan Medoxomil 20 mg/1
Uses, dosage, side effects and warnings for Amlodipine and Olmesartan Medoxomil →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 65862-854-30 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-854-30) | May 15, 2017 |
Recalls mentioning this NDC
- D-0289-2019 Dec 12, 2018 · Class III
Discoloration: This product is being recalled due to a confirmed pharmacist report that tablets from this lot were a pink color instead of cream (peach).
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