Package 72189-535-30

Brand: amantadine hcl

Generic: amantadine hcl
NDC Package

Package Facts

Identity

Package NDC 72189-535-30
Digits Only 7218953530
Product NDC 72189-535
Description

30 TABLET in 1 BOTTLE (72189-535-30)

Marketing

Marketing Status
Marketed Since 2024-02-23
Brand amantadine hcl
Generic amantadine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "12894d87-0c1f-831b-e063-6294a90af11d", "openfda": {"unii": ["M6Q1EO9TD0"], "rxcui": ["849395"], "spl_set_id": ["1211ebf4-3169-20ca-e063-6294a90aee4d"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-535-30)", "package_ndc": "72189-535-30", "marketing_start_date": "20240223"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-535-90)", "package_ndc": "72189-535-90", "marketing_start_date": "20240223"}], "brand_name": "Amantadine HCL", "product_id": "72189-535_12894d87-0c1f-831b-e063-6294a90af11d", "dosage_form": "TABLET", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "72189-535", "generic_name": "Amantadine HCL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amantadine HCL", "active_ingredients": [{"name": "AMANTADINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA209035", "marketing_category": "ANDA", "marketing_start_date": "20240223", "listing_expiration_date": "20261231"}