Package 39822-0190-1

Brand: acetazolamide

Generic: acetazolamide
NDC Package

Package Facts

Identity

Package NDC 39822-0190-1
Digits Only 3982201901
Product NDC 39822-0190
Description

1 VIAL, GLASS in 1 CARTON (39822-0190-1) / 5 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2009-03-01
Brand acetazolamide
Generic acetazolamide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "36974f91-0025-447d-e063-6294a90a0dc2", "openfda": {"unii": ["429ZT169UH"], "rxcui": ["307702"], "spl_set_id": ["a9199d3c-ce52-4db5-aa36-408f4e15e344"], "manufacturer_name": ["XGen Pharmaceuticals DJB, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (39822-0190-1)  / 5 mL in 1 VIAL, GLASS", "package_ndc": "39822-0190-1", "marketing_start_date": "20090301"}], "brand_name": "Acetazolamide", "product_id": "39822-0190_36974f91-0025-447d-e063-6294a90a0dc2", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "39822-0190", "generic_name": "Acetazolamide", "labeler_name": "XGen Pharmaceuticals DJB, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetazolamide", "active_ingredients": [{"name": "ACETAZOLAMIDE SODIUM", "strength": "500 mg/5mL"}], "application_number": "ANDA040784", "marketing_category": "ANDA", "marketing_start_date": "20081210", "listing_expiration_date": "20261231"}