NDC 33342-058 – Irbesartan and Hydrochlorothiazide
Irbesartan 300 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC33342-058
Product details
- Brand name
- Irbesartan and Hydrochlorothiazide
- Generic name
- Irbesartan and Hydrochlorothiazide
- Labeler
- Macleods Pharmaceuticals Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202414
- Marketed since
- September 27, 2012
- Listing expires
- December 31, 2026
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 33342-058-06 | 3 BLISTER PACK in 1 CARTON (33342-058-06) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Sep 27, 2012 |
| 33342-058-07 | 30 TABLET, FILM COATED in 1 BOTTLE (33342-058-07) | Sep 27, 2012 |
| 33342-058-10 | 90 TABLET, FILM COATED in 1 BOTTLE (33342-058-10) | Sep 27, 2012 |
| 33342-058-15 | 500 TABLET, FILM COATED in 1 BOTTLE (33342-058-15) | Sep 27, 2012 |
| 33342-058-39 | 9 BLISTER PACK in 1 CARTON (33342-058-39) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Sep 27, 2012 |
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