NDC 0517-1820 – Chlorothiazide Sodium
Chlorothiazide Sodium 500 mg/18mL · Injection, Powder, Lyophilized, For Solution · Intravenous
Product NDC0517-1820
Product details
- Brand name
- Chlorothiazide Sodium
- Generic name
- Chlorothiazide Sodium
- Labeler
- American Regent, Inc.
- Dosage form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA202561
- Marketed since
- April 1, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- Thiazide Diuretic
Active ingredients
- Chlorothiazide Sodium 500 mg/18mL
Uses, dosage, side effects and warnings for Chlorothiazide Sodium →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0517-1820-01 | 1 VIAL in 1 CARTON (0517-1820-01) / 18 mL in 1 VIAL | Apr 1, 2015 |
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