NDC 72162-1035 – Irbesartan and Hydrochlorothiazide
Irbesartan 150 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC72162-1035
Product details
- Brand name
- Irbesartan and Hydrochlorothiazide
- Generic name
- Irbesartan and Hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077369
- Marketed since
- January 24, 2013
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Irbesartan 150 mg/1
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Irbesartan and Hydrochlorothiazide →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 72162-1035-9 | 90 TABLET, FILM COATED in 1 BOTTLE (72162-1035-9) | Apr 7, 2026 |
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