Package 70954-033-20

Brand: acetazolamide

Generic: acetazolamide
NDC Package

Package Facts

Identity

Package NDC 70954-033-20
Digits Only 7095403320
Product NDC 70954-033
Description

1000 TABLET in 1 BOTTLE (70954-033-20)

Marketing

Marketing Status
Marketed Since 2019-10-17
Brand acetazolamide
Generic acetazolamide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bf074cfc-87f3-4328-a251-65f3f9d8556e", "openfda": {"nui": ["N0000175517", "N0000000235", "M0020790"], "upc": ["0370954033301", "0370954034308"], "unii": ["O3FX965V0I"], "rxcui": ["197303", "197304"], "spl_set_id": ["bde94a48-05d0-45a0-a589-ec05b7d16532"], "pharm_class_cs": ["Sulfonamides [CS]"], "pharm_class_epc": ["Carbonic Anhydrase Inhibitor [EPC]"], "pharm_class_moa": ["Carbonic Anhydrase Inhibitors [MoA]"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70954-033-20)", "package_ndc": "70954-033-20", "marketing_start_date": "20191017"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (70954-033-30)", "package_ndc": "70954-033-30", "marketing_start_date": "20191017"}], "brand_name": "Acetazolamide", "product_id": "70954-033_bf074cfc-87f3-4328-a251-65f3f9d8556e", "dosage_form": "TABLET", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "70954-033", "generic_name": "Acetazolamide", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetazolamide", "active_ingredients": [{"name": "ACETAZOLAMIDE", "strength": "125 mg/1"}], "application_number": "ANDA210588", "marketing_category": "ANDA", "marketing_start_date": "20191017", "listing_expiration_date": "20271231"}