Package 50268-069-15

Brand: amantadine hcl

Generic: amantadine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-069-15
Digits Only 5026806915
Product NDC 50268-069
Description

50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-069-15) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (50268-069-11)

Marketing

Marketing Status
Marketed Since 2014-03-28
Brand amantadine hcl
Generic amantadine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38566e1f-b7b1-540f-e063-6394a90a2760", "openfda": {"unii": ["M6Q1EO9TD0"], "rxcui": ["849389"], "spl_set_id": ["461e6444-189e-62ed-6c61-1c36a04459c6"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-069-15)  / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK (50268-069-11)", "package_ndc": "50268-069-15", "marketing_start_date": "20140328"}], "brand_name": "Amantadine HCl", "product_id": "50268-069_38566e1f-b7b1-540f-e063-6394a90a2760", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "50268-069", "generic_name": "AMANTADINE HYDROCHLORIDE", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amantadine HCl", "active_ingredients": [{"name": "AMANTADINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA078720", "marketing_category": "ANDA", "marketing_start_date": "20140328", "listing_expiration_date": "20261231"}