NDC 67877-447 – Olmesartan Medoxomil
Olmesartan Medoxomil 40 mg/1 · Tablet, Coated · Oral
Product NDC67877-447
Product details
- Brand name
- Olmesartan Medoxomil
- Generic name
- Olmesartan Medoxomil
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet, Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA206763
- Marketed since
- April 24, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker
Active ingredients
- Olmesartan Medoxomil 40 mg/1
Uses, dosage, side effects and warnings for Olmesartan Medoxomil →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 67877-447-05 | 500 TABLET, COATED in 1 BOTTLE (67877-447-05) | Apr 24, 2017 |
| 67877-447-10 | 1000 TABLET, COATED in 1 BOTTLE (67877-447-10) | Apr 24, 2017 |
| 67877-447-30 | 30 TABLET, COATED in 1 BOTTLE (67877-447-30) | Apr 24, 2017 |
| 67877-447-90 | 90 TABLET, COATED in 1 BOTTLE (67877-447-90) | Apr 24, 2017 |
Recalls mentioning this NDC
- D-0392-2021 Jun 2, 2021 · Class III
Presence of Foreign Tablet/Capsule - D-0828-2020 Feb 12, 2020 · Class II
cGMP Deviations; Olmesartan Medoximil Tablets 20 mg was released in error with alternate API source prior to filing and approval of Prior Approval Supplement.
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