NDC 23155-009 – Hydrochlorothiazide
Hydrochlorothiazide 50 mg/1 · Tablet · Oral
Product NDC23155-009
Product details
- Brand name
- Hydrochlorothiazide
- Generic name
- Hydrochlorothiazide
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA085182
- Marketed since
- January 15, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Thiazide Diuretic
Active ingredients
- Hydrochlorothiazide 50 mg/1
Uses, dosage, side effects and warnings for Hydrochlorothiazide →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 23155-009-01 | 100 TABLET in 1 BOTTLE (23155-009-01) | Jan 15, 2015 |
| 23155-009-05 | 500 TABLET in 1 BOTTLE (23155-009-05) | Jan 15, 2015 |
| 23155-009-10 | 1000 TABLET in 1 BOTTLE (23155-009-10) | Jan 15, 2015 |
| 23155-009-18 | 5000 TABLET in 1 BOTTLE (23155-009-18) | Feb 1, 2015 |
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