Package 51672-4022-1

Brand: acetazolamide

Generic: acetazolamide
NDC Package

Package Facts

Identity

Package NDC 51672-4022-1
Digits Only 5167240221
Product NDC 51672-4022
Product ID 51672-4022_31e42345-2444-92e6-e063-6394a90ae741
Description

100 TABLET in 1 BOTTLE (51672-4022-1)

Marketing

Marketing Status
Marketed Since 1997-05-28
Brand acetazolamide
Generic acetazolamide
Sample Package No

Linked Drug Pages (1)

Acetazolamide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "31e42345-2444-92e6-e063-6394a90ae741", "openfda": {"nui": ["N0000175517", "N0000000235", "M0020790"], "upc": ["0351672402211"], "unii": ["O3FX965V0I"], "rxcui": ["197303", "197304"], "spl_set_id": ["abeb13eb-66a5-4030-9bc2-5981acd196b9"], "pharm_class_cs": ["Sulfonamides [CS]"], "pharm_class_epc": ["Carbonic Anhydrase Inhibitor [EPC]"], "pharm_class_moa": ["Carbonic Anhydrase Inhibitors [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (51672-4022-1)", "package_ndc": "51672-4022-1", "marketing_start_date": "19970528"}], "brand_name": "Acetazolamide", "product_id": "51672-4022_31e42345-2444-92e6-e063-6394a90ae741", "dosage_form": "TABLET", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "51672-4022", "generic_name": "Acetazolamide", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetazolamide", "active_ingredients": [{"name": "ACETAZOLAMIDE", "strength": "125 mg/1"}], "application_number": "ANDA040195", "marketing_category": "ANDA", "marketing_start_date": "19970528", "listing_expiration_date": "20261231"}