NDC 71335-1481 – Hydrochlorothiazide
Hydrochlorothiazide 25 mg/1 · Tablet · Oral
Product NDC71335-1481
Product details
- Brand name
- Hydrochlorothiazide
- Generic name
- Hydrochlorothiazide
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA040412
- Marketed since
- March 29, 2002
- 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 |
|---|---|---|
| 71335-1481-0 | 120 TABLET in 1 BOTTLE (71335-1481-0) | Mar 29, 2002 |
| 71335-1481-1 | 100 TABLET in 1 BOTTLE (71335-1481-1) | Mar 29, 2002 |
| 71335-1481-2 | 30 TABLET in 1 BOTTLE (71335-1481-2) | Mar 29, 2002 |
| 71335-1481-3 | 7 TABLET in 1 BOTTLE (71335-1481-3) | Mar 29, 2002 |
| 71335-1481-4 | 14 TABLET in 1 BOTTLE (71335-1481-4) | Mar 29, 2002 |
| 71335-1481-5 | 60 TABLET in 1 BOTTLE (71335-1481-5) | Mar 29, 2002 |
| 71335-1481-6 | 2 TABLET in 1 BOTTLE (71335-1481-6) | Mar 29, 2002 |
| 71335-1481-7 | 90 TABLET in 1 BOTTLE (71335-1481-7) | Mar 29, 2002 |
| 71335-1481-8 | 4 TABLET in 1 BOTTLE (71335-1481-8) | Mar 29, 2002 |
| 71335-1481-9 | 8 TABLET in 1 BOTTLE (71335-1481-9) | Mar 29, 2002 |
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