NDC 72162-2317 – Irbesartan and Hydrochlorothiazide
Irbesartan 150 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral
Product NDC72162-2317
Product details
- Brand name
- Irbesartan and Hydrochlorothiazide
- Generic name
- Irbesartan and Hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA203072
- Marketed since
- March 1, 2014
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 72162-2317-3 | 30 TABLET in 1 BOTTLE (72162-2317-3) | Mar 1, 2014 |
| 72162-2317-9 | 90 TABLET in 1 BOTTLE (72162-2317-9) | Mar 1, 2014 |
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