Package 25021-305-66

Brand: chlorothiazide sodium

Generic: chlorothiazide sodium
NDC Package

Package Facts

Identity

Package NDC 25021-305-66
Digits Only 2502130566
Product NDC 25021-305
Product ID 25021-305_09b4e4be-edc0-4a5e-abb2-1572287f2abe
Description

1 VIAL in 1 CARTON (25021-305-66) / 18 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2019-12-15
Brand chlorothiazide sodium
Generic chlorothiazide sodium
Sample Package No

Linked Drug Pages (1)

chlorothiazide sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "09b4e4be-edc0-4a5e-abb2-1572287f2abe", "openfda": {"unii": ["SN86FG7N2K"], "rxcui": ["484152"], "spl_set_id": ["82dd0bdd-e6bd-48ea-8f58-c8bf71bbfe2c"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (25021-305-66)  / 18 mL in 1 VIAL", "package_ndc": "25021-305-66", "marketing_start_date": "20191215"}], "brand_name": "chlorothiazide sodium", "product_id": "25021-305_09b4e4be-edc0-4a5e-abb2-1572287f2abe", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "25021-305", "generic_name": "chlorothiazide sodium", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "chlorothiazide sodium", "active_ingredients": [{"name": "CHLOROTHIAZIDE SODIUM", "strength": "500 mg/18mL"}], "application_number": "ANDA202462", "marketing_category": "ANDA", "marketing_start_date": "20191215", "listing_expiration_date": "20261231"}