NDC 68083-614 – Chlorothiazide sodium
Chlorothiazide Sodium 500 mg/18mL · Injection, Powder, Lyophilized, For Solution · Intravenous
Product NDC68083-614
Product details
- Brand name
- Chlorothiazide sodium
- Generic name
- Chlorothiazide sodium
- Labeler
- Gland Pharma Limited
- Dosage form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA218630
- Marketed since
- October 3, 2024
- 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 |
|---|---|---|
| 68083-614-01 | 1 VIAL in 1 CARTON (68083-614-01) / 18 mL in 1 VIAL | Oct 3, 2024 |
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