NDC 71335-1976 – Hydrochlorothiazide
Hydrochlorothiazide 50 mg/1 · Tablet · Oral
Product NDC71335-1976
Product details
- Brand name
- Hydrochlorothiazide
- Generic name
- Hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA040907
- Marketed since
- August 15, 2008
- 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 (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1976-0 | 45 TABLET in 1 BOTTLE (71335-1976-0) | Dec 21, 2021 |
| 71335-1976-1 | 30 TABLET in 1 BOTTLE (71335-1976-1) | Oct 15, 2021 |
| 71335-1976-2 | 60 TABLET in 1 BOTTLE (71335-1976-2) | Dec 21, 2021 |
| 71335-1976-3 | 90 TABLET in 1 BOTTLE (71335-1976-3) | Dec 3, 2021 |
| 71335-1976-4 | 28 TABLET in 1 BOTTLE (71335-1976-4) | Dec 21, 2021 |
| 71335-1976-5 | 56 TABLET in 1 BOTTLE (71335-1976-5) | Dec 21, 2021 |
| 71335-1976-6 | 100 TABLET in 1 BOTTLE (71335-1976-6) | Dec 21, 2021 |
| 71335-1976-7 | 7 TABLET in 1 BOTTLE (71335-1976-7) | Dec 21, 2021 |
| 71335-1976-8 | 14 TABLET in 1 BOTTLE (71335-1976-8) | Dec 21, 2021 |
| 71335-1976-9 | 120 TABLET in 1 BOTTLE (71335-1976-9) | Dec 21, 2021 |
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