NDC 72789-512 – Hydrochlorothiazide
Hydrochlorothiazide 25 mg/1 · Tablet · Oral
Product NDC72789-512
Product details
- Brand name
- Hydrochlorothiazide
- Generic name
- Hydrochlorothiazide
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA083177
- Marketed since
- January 12, 1973
- Listing expires
- December 31, 2026
- Pharmacologic class
- Thiazide Diuretic
Active ingredients
- Hydrochlorothiazide 25 mg/1
Uses, dosage, side effects and warnings for Hydrochlorothiazide →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 72789-512-30 | 30 TABLET in 1 BOTTLE, PLASTIC (72789-512-30) | Jun 6, 2025 |
| 72789-512-60 | 60 TABLET in 1 BOTTLE, PLASTIC (72789-512-60) | Oct 29, 2025 |
| 72789-512-90 | 90 TABLET in 1 BOTTLE, PLASTIC (72789-512-90) | Jun 6, 2025 |
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