NDC 33342-192 – AMLODIPINE and OLMESARTAN medoxomil
Amlodipine Besylate 10 mg/1; Olmesartan Medoxomil 20 mg/1 · Tablet, Film Coated · Oral
Product NDC33342-192
Product details
- Brand name
- AMLODIPINE and OLMESARTAN medoxomil
- Generic name
- AMLODIPINE and OLMESARTAN medoxomil
- Labeler
- Macleods Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA206884
- Marketed since
- October 27, 2016
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Calcium Channel Blocker; Dihydropyridine Calcium Channel Blocker
Active ingredients
- Amlodipine Besylate 10 mg/1
- Olmesartan Medoxomil 20 mg/1
Uses, dosage, side effects and warnings for Amlodipine and Olmesartan Medoxomil →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 33342-192-07 | 30 TABLET, FILM COATED in 1 BOTTLE (33342-192-07) | Oct 27, 2016 |
| 33342-192-10 | 90 TABLET, FILM COATED in 1 BOTTLE (33342-192-10) | Oct 27, 2016 |
| 33342-192-12 | 10 BLISTER PACK in 1 CARTON (33342-192-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Oct 27, 2016 |
| 33342-192-44 | 1000 TABLET, FILM COATED in 1 BOTTLE (33342-192-44) | Oct 27, 2016 |
Recalls mentioning this NDC
- D-0632-2022 Mar 9, 2022 · Class II
cGMP deviations - D-0509-2021 Jun 2, 2021 · Class II
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
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