Package 71335-2959-1

Brand: amantadine hydrochloride

Generic: amantadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2959-1
Digits Only 7133529591
Product NDC 71335-2959
Description

100 CAPSULE in 1 BOTTLE (71335-2959-1)

Marketing

Marketing Status
Marketed Since 2025-10-22
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": "99e43d39-01e6-445c-a222-78b4fb8b5cd3", "openfda": {"unii": ["M6Q1EO9TD0"], "rxcui": ["849389"], "spl_set_id": ["96aefbca-fe71-42ef-8079-d0d9e7370ccb"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (71335-2959-1)", "package_ndc": "71335-2959-1", "marketing_start_date": "20251022"}], "brand_name": "Amantadine Hydrochloride", "product_id": "71335-2959_99e43d39-01e6-445c-a222-78b4fb8b5cd3", "dosage_form": "CAPSULE", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "71335-2959", "generic_name": "Amantadine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amantadine Hydrochloride", "active_ingredients": [{"name": "AMANTADINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA209171", "marketing_category": "ANDA", "marketing_start_date": "20170612", "listing_expiration_date": "20261231"}