0517-1820Level 3
Chlorothiazide Sodium (Chlorothiazide Sodium)
**Product type:** Human Prescription Drug
**Active ingredient:** CHLOROTHIAZIDE SODIUM
**Strength:** 500 mg/18mL
**Dosage form:** Injection, Powder, Lyophilized, For Solution
**Route:** Intravenous
**Labeler:** American Regent, Inc.
**Marketing category:** ANDA (ANDA202561)
**Pharmacologic class:** Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
GET
/api/v1/systems/ndc_fda/nodes/0517-1820Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.