Package 0591-4920-01

Brand: amantadine hydrochloride

Generic: amantadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0591-4920-01
Digits Only 0591492001
Product NDC 0591-4920
Description

100 TABLET in 1 BOTTLE (0591-4920-01)

Marketing

Marketing Status
Discontinued 2026-06-30
Brand amantadine hydrochloride
Generic amantadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "67ce5a52-d507-4333-b0a0-b7177f896aec", "openfda": {"unii": ["M6Q1EO9TD0"], "rxcui": ["849395"], "spl_set_id": ["d9c9eaf7-dcc7-49c1-99d4-49f4dac3779f"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0591-4920-01)", "package_ndc": "0591-4920-01", "marketing_end_date": "20260630", "marketing_start_date": "20170103"}], "brand_name": "Amantadine Hydrochloride", "product_id": "0591-4920_67ce5a52-d507-4333-b0a0-b7177f896aec", "dosage_form": "TABLET", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "0591-4920", "generic_name": "Amantadine Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amantadine Hydrochloride", "active_ingredients": [{"name": "AMANTADINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA208096", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20170103"}