NDC 65862-134 – Hydrochlorothiazide
Hydrochlorothiazide 50 mg/1 · Tablet · Oral
Product NDC65862-134
Product details
- Brand name
- Hydrochlorothiazide
- Generic name
- Hydrochlorothiazide
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA040780
- Marketed since
- July 20, 2007
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 65862-134-01 | 100 TABLET in 1 BOTTLE (65862-134-01) | Jul 20, 2007 |
| 65862-134-99 | 1000 TABLET in 1 BOTTLE (65862-134-99) | Jul 20, 2007 |
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