NDC 65862-629 – Irbesartan and Hydrochlorothiazide
Irbesartan 150 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-629
Product details
- Brand name
- Irbesartan and Hydrochlorothiazide
- Generic name
- Irbesartan and Hydrochlorothiazide
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203630
- Marketed since
- February 22, 2013
- Listing expires
- December 31, 2026
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 65862-629-05 | 500 TABLET, FILM COATED in 1 BOTTLE (65862-629-05) | Feb 22, 2013 |
| 65862-629-30 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-629-30) | Feb 22, 2013 |
| 65862-629-90 | 90 TABLET, FILM COATED in 1 BOTTLE (65862-629-90) | Feb 22, 2013 |
| 65862-629-99 | 1000 TABLET, FILM COATED in 1 BOTTLE (65862-629-99) | Feb 22, 2013 |
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