Package 68083-614-01

Brand: chlorothiazide sodium

Generic: chlorothiazide sodium
NDC Package

Package Facts

Identity

Package NDC 68083-614-01
Digits Only 6808361401
Product NDC 68083-614
Product ID 68083-614_e19fe503-9b2e-4db0-b4ee-0fb9ec9c11c2
Description

1 VIAL in 1 CARTON (68083-614-01) / 18 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2024-10-03
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": "e19fe503-9b2e-4db0-b4ee-0fb9ec9c11c2", "openfda": {"upc": ["0368083614010"], "unii": ["SN86FG7N2K"], "rxcui": ["484152"], "spl_set_id": ["bf921935-9740-458e-b786-69f76d8ad139"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (68083-614-01)  / 18 mL in 1 VIAL", "package_ndc": "68083-614-01", "marketing_start_date": "20241003"}], "brand_name": "Chlorothiazide sodium", "product_id": "68083-614_e19fe503-9b2e-4db0-b4ee-0fb9ec9c11c2", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "68083-614", "generic_name": "Chlorothiazide sodium", "labeler_name": "Gland Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorothiazide sodium", "active_ingredients": [{"name": "CHLOROTHIAZIDE SODIUM", "strength": "500 mg/18mL"}], "application_number": "ANDA218630", "marketing_category": "ANDA", "marketing_start_date": "20241003", "listing_expiration_date": "20261231"}