NDC 71335-9647 – Hydrochlorothiazide
Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral
Product NDC71335-9647
Product details
- Brand name
- Hydrochlorothiazide
- Generic name
- Hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA040702
- Marketed since
- November 1, 2019
- Listing expires
- December 31, 2027
- Pharmacologic class
- Thiazide Diuretic
Active ingredients
- Hydrochlorothiazide 12.5 mg/1
Uses, dosage, side effects and warnings for Hydrochlorothiazide →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 71335-9647-1 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-9647-1) | Feb 20, 2024 |
| 71335-9647-2 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-9647-2) | Jul 20, 2023 |
| 71335-9647-3 | 14 TABLET in 1 BOTTLE, PLASTIC (71335-9647-3) | Sep 6, 2024 |
| 71335-9647-4 | 100 TABLET in 1 BOTTLE, PLASTIC (71335-9647-4) | Sep 6, 2024 |
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