NDC 71205-090 – Hydrochlorothiazide
Hydrochlorothiazide 50 mg/1 · Tablet · Oral
Product NDC71205-090
Product details
- Brand name
- Hydrochlorothiazide
- Generic name
- Hydrochlorothiazide
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA202556
- Marketed since
- April 10, 2013
- 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 (7)
| Package NDC | Description | Since |
|---|---|---|
| 71205-090-00 | 100 TABLET in 1 BOTTLE (71205-090-00) | Aug 1, 2018 |
| 71205-090-03 | 3 TABLET in 1 BOTTLE (71205-090-03) | Aug 1, 2018 |
| 71205-090-07 | 7 TABLET in 1 BOTTLE (71205-090-07) | Aug 1, 2018 |
| 71205-090-10 | 10 TABLET in 1 BOTTLE (71205-090-10) | Aug 1, 2018 |
| 71205-090-30 | 30 TABLET in 1 BOTTLE (71205-090-30) | Aug 1, 2018 |
| 71205-090-60 | 60 TABLET in 1 BOTTLE (71205-090-60) | Aug 1, 2018 |
| 71205-090-90 | 90 TABLET in 1 BOTTLE (71205-090-90) | Aug 1, 2018 |
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