Package 72162-2566-6

Brand: galantamine

Generic: galantamine
NDC Package

Package Facts

Identity

Package NDC 72162-2566-6
Digits Only 7216225666
Product NDC 72162-2566
Description

60 TABLET, FILM COATED in 1 BOTTLE (72162-2566-6)

Marketing

Marketing Status
Marketed Since 2025-11-04
Brand galantamine
Generic galantamine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cf937559-bf6e-4dfd-b651-7b8fcb839e36", "openfda": {"unii": ["MJ4PTD2VVW"], "rxcui": ["310437"], "spl_set_id": ["694ea1a5-153a-4145-9910-a0a1dc4ddbcc"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (72162-2566-6)", "package_ndc": "72162-2566-6", "marketing_start_date": "20251104"}], "brand_name": "Galantamine", "product_id": "72162-2566_cf937559-bf6e-4dfd-b651-7b8fcb839e36", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "72162-2566", "generic_name": "Galantamine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Galantamine", "active_ingredients": [{"name": "GALANTAMINE HYDROBROMIDE", "strength": "8 mg/1"}], "application_number": "ANDA090957", "marketing_category": "ANDA", "marketing_start_date": "20110329", "listing_expiration_date": "20261231"}