Package 50268-036-14

Brand: amantadine

Generic: amantadine
NDC Package

Package Facts

Identity

Package NDC 50268-036-14
Digits Only 5026803614
Product NDC 50268-036
Description

40 TRAY in 1 CASE (50268-036-14) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (50268-036-11)

Marketing

Marketing Status
Marketed Since 2026-01-19
Brand amantadine
Generic amantadine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48c949ef-d92b-abba-e063-6394a90a2d2a", "openfda": {"unii": ["M6Q1EO9TD0"], "rxcui": ["849385"], "spl_set_id": ["48c949e3-86e0-c639-e063-6294a90acdba"], "manufacturer_name": ["AvPAK"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "40 TRAY in 1 CASE (50268-036-14)  / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (50268-036-11)", "package_ndc": "50268-036-14", "marketing_start_date": "20260119"}], "brand_name": "Amantadine", "product_id": "50268-036_48c949ef-d92b-abba-e063-6394a90a2d2a", "dosage_form": "SOLUTION", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "50268-036", "generic_name": "Amantadine", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amantadine", "active_ingredients": [{"name": "AMANTADINE HYDROCHLORIDE", "strength": "50 mg/5mL"}], "application_number": "ANDA075060", "marketing_category": "ANDA", "marketing_start_date": "20260119", "listing_expiration_date": "20271231"}