Package 10135-692-05

Brand: amantadine hydrochloride

Generic: amantadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10135-692-05
Digits Only 1013569205
Product NDC 10135-692
Description

500 TABLET in 1 BOTTLE (10135-692-05)

Marketing

Marketing Status
Marketed Since 2020-03-01
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": "3e752827-026e-d525-e063-6394a90a7e80", "openfda": {"unii": ["M6Q1EO9TD0"], "rxcui": ["849389", "849395"], "spl_set_id": ["25af52ee-9b29-4c07-a383-62d4537b63e0"], "manufacturer_name": ["Marlex Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10135-692-01)", "package_ndc": "10135-692-01", "marketing_start_date": "20200301"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (10135-692-05)", "package_ndc": "10135-692-05", "marketing_start_date": "20200301"}], "brand_name": "Amantadine Hydrochloride", "product_id": "10135-692_3e752827-026e-d525-e063-6394a90a7e80", "dosage_form": "TABLET", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "10135-692", "generic_name": "Amantadine Hydrochloride", "labeler_name": "Marlex Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amantadine Hydrochloride", "active_ingredients": [{"name": "AMANTADINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA210215", "marketing_category": "ANDA", "marketing_start_date": "20200301", "listing_expiration_date": "20261231"}