NDC 46708-442 – Irbesartan and Hydrochlorothiazide
Irbesartan 150 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral
Product NDC46708-442
Product details
- Brand name
- Irbesartan and Hydrochlorothiazide
- Generic name
- Irbesartan and Hydrochlorothiazide
- Labeler
- Alembic Pharmaceuticals Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA091370
- Marketed since
- May 23, 2016
- 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 |
|---|---|---|
| 46708-442-10 | 10 TABLET in 1 BLISTER PACK (46708-442-10) | May 23, 2016 |
| 46708-442-30 | 30 TABLET in 1 BOTTLE (46708-442-30) | May 23, 2016 |
| 46708-442-90 | 90 TABLET in 1 BOTTLE (46708-442-90) | May 23, 2016 |
| 46708-442-91 | 1000 TABLET in 1 BOTTLE (46708-442-91) | May 23, 2016 |
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