NDC 47335-330 – Chlorothiazide Sodium
Chlorothiazide Sodium 500 mg/18mL · Injection, Powder, Lyophilized, For Solution · Intravenous
Product NDC47335-330
Product details
- Brand name
- Chlorothiazide Sodium
- Generic name
- Chlorothiazide Sodium
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA091546
- Marketed since
- August 25, 2016
- 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 |
|---|---|---|
| 47335-330-40 | 1 VIAL, SINGLE-DOSE in 1 CARTON (47335-330-40) / 18 mL in 1 VIAL, SINGLE-DOSE | Aug 25, 2016 |
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