Package 67457-853-50

Brand: acetazolamide

Generic: acetazolamide sodium
NDC Package

Package Facts

Identity

Package NDC 67457-853-50
Digits Only 6745785350
Product NDC 67457-853
Description

1 VIAL in 1 CARTON (67457-853-50) / 5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2018-09-13
Brand acetazolamide
Generic acetazolamide sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "300661cb-a5d8-4edc-a191-72284744e1eb", "openfda": {"unii": ["429ZT169UH"], "rxcui": ["307702"], "spl_set_id": ["521838b0-a10d-495f-a014-f9ff25a6b6f3"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (67457-853-50)  / 5 mL in 1 VIAL", "package_ndc": "67457-853-50", "marketing_start_date": "20180913"}], "brand_name": "Acetazolamide", "product_id": "67457-853_300661cb-a5d8-4edc-a191-72284744e1eb", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "67457-853", "generic_name": "acetazolamide sodium", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetazolamide", "active_ingredients": [{"name": "ACETAZOLAMIDE SODIUM", "strength": "500 mg/5mL"}], "application_number": "ANDA200880", "marketing_category": "ANDA", "marketing_start_date": "20180913", "listing_expiration_date": "20261231"}