NDC 65862-779 – Olmesartan Medoxomil and Hydrochlorothiazide
Olmesartan Medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-779
Product details
- Brand name
- Olmesartan Medoxomil and Hydrochlorothiazide
- Generic name
- Olmesartan Medoxomil and Hydrochlorothiazide
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA205391
- Marketed since
- April 24, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Olmesartan Medoxomil 20 mg/1
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Olmesartan Medoxomil And Hydrochlorothiazide →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 65862-779-30 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-779-30) | Apr 24, 2017 |
| 65862-779-78 | 10 BLISTER PACK in 1 CARTON (65862-779-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-779-10) | Apr 24, 2017 |
| 65862-779-90 | 90 TABLET, FILM COATED in 1 BOTTLE (65862-779-90) | Apr 24, 2017 |
| 65862-779-99 | 1000 TABLET, FILM COATED in 1 BOTTLE (65862-779-99) | Apr 24, 2017 |
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