NDC 71335-0269 – Hydrochlorothiazide
Hydrochlorothiazide 25 mg/1 · Tablet · Oral
Product NDC71335-0269
Product details
- Brand name
- Hydrochlorothiazide
- Generic name
- Hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA202556
- Marketed since
- April 10, 2013
- Listing expires
- December 31, 2027
- Pharmacologic class
- Thiazide Diuretic
Active ingredients
- Hydrochlorothiazide 25 mg/1
Uses, dosage, side effects and warnings for Hydrochlorothiazide →
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0269-0 | 120 TABLET in 1 BOTTLE (71335-0269-0) | Feb 9, 2022 |
| 71335-0269-1 | 100 TABLET in 1 BOTTLE (71335-0269-1) | Feb 9, 2022 |
| 71335-0269-2 | 30 TABLET in 1 BOTTLE (71335-0269-2) | Feb 9, 2022 |
| 71335-0269-3 | 7 TABLET in 1 BOTTLE (71335-0269-3) | Feb 9, 2022 |
| 71335-0269-4 | 14 TABLET in 1 BOTTLE (71335-0269-4) | Feb 9, 2022 |
| 71335-0269-5 | 60 TABLET in 1 BOTTLE (71335-0269-5) | Feb 9, 2022 |
| 71335-0269-6 | 2 TABLET in 1 BOTTLE (71335-0269-6) | Feb 9, 2022 |
| 71335-0269-7 | 90 TABLET in 1 BOTTLE (71335-0269-7) | Feb 9, 2022 |
| 71335-0269-8 | 4 TABLET in 1 BOTTLE (71335-0269-8) | Feb 9, 2022 |
| 71335-0269-9 | 8 TABLET in 1 BOTTLE (71335-0269-9) | Feb 9, 2022 |
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