NDC 16729-366 – Olmesartan Medoxomil And Hydrochlorothiazide
Olmesartan Medoxomil 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC16729-366
Product details
- Brand name
- Olmesartan Medoxomil And Hydrochlorothiazide
- Generic name
- Olmesartan Medoxomil And Hydrochlorothiazide
- Labeler
- Accord Healthcare Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209281
- Marketed since
- September 21, 2020
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 16729-366-15 | 90 TABLET, FILM COATED in 1 BOTTLE (16729-366-15) | Sep 21, 2020 |
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