NDC 82804-972 – Hydrochlorothiazide
Hydrochlorothiazide 25 mg/1 · Tablet · Oral
Product NDC82804-972
Product details
- Brand name
- Hydrochlorothiazide
- Generic name
- Hydrochlorothiazide
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA087059
- Marketed since
- September 25, 2020
- 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 (7)
| Package NDC | Description | Since |
|---|---|---|
| 82804-972-00 | 100 TABLET in 1 BOTTLE (82804-972-00) | Feb 13, 2025 |
| 82804-972-11 | 1000 TABLET in 1 BOTTLE (82804-972-11) | Feb 13, 2025 |
| 82804-972-30 | 30 TABLET in 1 BOTTLE (82804-972-30) | Feb 13, 2025 |
| 82804-972-55 | 500 TABLET in 1 BOTTLE (82804-972-55) | Feb 13, 2025 |
| 82804-972-60 | 60 TABLET in 1 BOTTLE (82804-972-60) | Feb 13, 2025 |
| 82804-972-72 | 120 TABLET in 1 BOTTLE (82804-972-72) | Feb 13, 2025 |
| 82804-972-90 | 90 TABLET in 1 BOTTLE (82804-972-90) | Feb 13, 2025 |
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