Package 62135-609-90

Brand: amantadine hydrochloride

Generic: amantadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-609-90
Digits Only 6213560990
Product NDC 62135-609
Description

90 CAPSULE in 1 BOTTLE (62135-609-90)

Marketing

Marketing Status
Marketed Since 2023-06-29
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": "2424250c-0ccb-d7b0-e063-6394a90a63b7", "openfda": {"upc": ["0362135609900"], "unii": ["M6Q1EO9TD0"], "rxcui": ["849389"], "spl_set_id": ["a016ab57-d18f-4a3b-b2ab-f91fecc1eef7"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE in 1 BOTTLE (62135-609-90)", "package_ndc": "62135-609-90", "marketing_start_date": "20230629"}], "brand_name": "Amantadine Hydrochloride", "product_id": "62135-609_2424250c-0ccb-d7b0-e063-6394a90a63b7", "dosage_form": "CAPSULE", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "62135-609", "generic_name": "Amantadine Hydrochloride", "labeler_name": "Chartwell RX, LLC", "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"}