NDC 71335-1097 – Irbesartan and Hydrochlorothiazide
Irbesartan 150 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1097
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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1097-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1097-1) | Feb 12, 2019 |
| 71335-1097-2 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1097-2) | Mar 17, 2021 |
| 71335-1097-3 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-1097-3) | Apr 8, 2022 |
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