NDC 71335-0652 – Hydrochlorothiazide
Hydrochlorothiazide 25 mg/1 · Tablet · Oral
Product NDC71335-0652
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 25 mg/1
Uses, dosage, side effects and warnings for Hydrochlorothiazide →
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0652-0 | 8 TABLET in 1 BOTTLE (71335-0652-0) | Dec 27, 2021 |
| 71335-0652-1 | 100 TABLET in 1 BOTTLE (71335-0652-1) | Jan 21, 2021 |
| 71335-0652-2 | 30 TABLET in 1 BOTTLE (71335-0652-2) | Mar 9, 2018 |
| 71335-0652-3 | 7 TABLET in 1 BOTTLE (71335-0652-3) | Apr 11, 2018 |
| 71335-0652-4 | 14 TABLET in 1 BOTTLE (71335-0652-4) | Mar 15, 2021 |
| 71335-0652-5 | 60 TABLET in 1 BOTTLE (71335-0652-5) | Nov 16, 2021 |
| 71335-0652-6 | 2 TABLET in 1 BOTTLE (71335-0652-6) | Dec 27, 2021 |
| 71335-0652-7 | 90 TABLET in 1 BOTTLE (71335-0652-7) | Mar 14, 2018 |
| 71335-0652-8 | 4 TABLET in 1 BOTTLE (71335-0652-8) | May 10, 2018 |
| 71335-0652-9 | 6 TABLET in 1 BOTTLE (71335-0652-9) | Dec 27, 2021 |
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