NDC 68788-7790 – Hydrochlorothiazide
Hydrochlorothiazide 50 mg/1 · Tablet · Oral
Product NDC68788-7790
Product details
- Brand name
- Hydrochlorothiazide
- Generic name
- Hydrochlorothiazide
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA085182
- Marketed since
- October 21, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Thiazide Diuretic
Active ingredients
- Hydrochlorothiazide 50 mg/1
Uses, dosage, side effects and warnings for Hydrochlorothiazide →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68788-7790-0 | 100 TABLET in 1 BOTTLE (68788-7790-0) | Oct 21, 2020 |
| 68788-7790-1 | 15 TABLET in 1 BOTTLE (68788-7790-1) | Oct 21, 2020 |
| 68788-7790-3 | 30 TABLET in 1 BOTTLE (68788-7790-3) | Oct 21, 2020 |
| 68788-7790-6 | 60 TABLET in 1 BOTTLE (68788-7790-6) | Oct 21, 2020 |
| 68788-7790-9 | 90 TABLET in 1 BOTTLE (68788-7790-9) | Oct 21, 2020 |
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