NDC 63323-658 – Chlorothiazide
Chlorothiazide Sodium 500 mg/18mL · Injection, Powder, Lyophilized, For Solution · Intravenous
Product NDC63323-658
Product details
- Brand name
- Chlorothiazide
- Generic name
- Chlorothiazide Sodium
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA090896
- Marketed since
- October 21, 2009
- Listing expires
- December 31, 2026
- Pharmacologic class
- Thiazide Diuretic
Active ingredients
- Chlorothiazide Sodium 500 mg/18mL
Uses, dosage, side effects and warnings for Chlorothiazide →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 63323-658-20 | 1 VIAL in 1 BOX (63323-658-20) / 18 mL in 1 VIAL | Oct 21, 2009 |
| 63323-658-27 | 1 VIAL in 1 BOX (63323-658-27) / 18 mL in 1 VIAL | Oct 21, 2009 |
| 63323-658-94 | 1 VIAL in 1 BOX (63323-658-94) / 18 mL in 1 VIAL | Oct 21, 2009 |