NDC 0093-8232 – Irbesartan and Hydrochlorothiazide
Irbesartan 300 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC0093-8232
Product details
- Brand name
- Irbesartan and Hydrochlorothiazide
- Generic name
- Irbesartan and Hydrochlorothiazide
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077369
- Marketed since
- August 27, 2013
- Listing expires
- December 31, 2027
- Pharmacologic class
- Angiotensin 2 Receptor Blocker; Thiazide Diuretic
Active ingredients
- Irbesartan 300 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 |
|---|---|---|
| 0093-8232-56 | 30 TABLET, FILM COATED in 1 BOTTLE (0093-8232-56) | Aug 27, 2013 |
| 0093-8232-98 | 90 TABLET, FILM COATED in 1 BOTTLE (0093-8232-98) | Aug 27, 2013 |
Recalls mentioning this NDC
- D-0521-2016 Dec 23, 2015 · Class III
Labeling: Incorrect or Missing Lot AND/OR Exp Date.
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