Package 71335-2215-3

Brand: acetazolamide

Generic: acetazolamide
NDC Package

Package Facts

Identity

Package NDC 71335-2215-3
Digits Only 7133522153
Product NDC 71335-2215
Description

10 TABLET in 1 BOTTLE (71335-2215-3)

Marketing

Marketing Status
Marketed Since 2023-08-15
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": "fe123006-9846-48a9-b743-b57cfe12af23", "openfda": {"nui": ["N0000175517", "N0000000235", "M0020790"], "unii": ["O3FX965V0I"], "rxcui": ["197304"], "spl_set_id": ["71f1fbbb-428e-4bf7-bc20-2946c1079bd3"], "pharm_class_cs": ["Sulfonamides [CS]"], "pharm_class_epc": ["Carbonic Anhydrase Inhibitor [EPC]"], "pharm_class_moa": ["Carbonic Anhydrase Inhibitors [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2215-1)", "package_ndc": "71335-2215-1", "marketing_start_date": "20230815"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2215-2)", "package_ndc": "71335-2215-2", "marketing_start_date": "20230815"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-2215-3)", "package_ndc": "71335-2215-3", "marketing_start_date": "20230815"}], "brand_name": "Acetazolamide", "product_id": "71335-2215_fe123006-9846-48a9-b743-b57cfe12af23", "dosage_form": "TABLET", "pharm_class": ["Carbonic Anhydrase Inhibitor [EPC]", "Carbonic Anhydrase Inhibitors [MoA]", "Sulfonamides [CS]"], "product_ndc": "71335-2215", "generic_name": "Acetazolamide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acetazolamide", "active_ingredients": [{"name": "ACETAZOLAMIDE", "strength": "250 mg/1"}], "application_number": "ANDA215101", "marketing_category": "ANDA", "marketing_start_date": "20210819", "listing_expiration_date": "20261231"}