Package 71335-2766-1

Brand: galantamine

Generic: galantamine
NDC Package

Package Facts

Identity

Package NDC 71335-2766-1
Digits Only 7133527661
Product NDC 71335-2766
Description

60 TABLET, FILM COATED in 1 BOTTLE (71335-2766-1)

Marketing

Marketing Status
Marketed Since 2025-10-03
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": "29de3c5e-581d-4ab9-b0eb-2218eff2e821", "openfda": {"unii": ["MJ4PTD2VVW"], "rxcui": ["310436"], "spl_set_id": ["261889d3-41c8-4655-98f7-41317778e7a1"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2766-1)", "package_ndc": "71335-2766-1", "marketing_start_date": "20251003"}], "brand_name": "Galantamine", "product_id": "71335-2766_29de3c5e-581d-4ab9-b0eb-2218eff2e821", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "71335-2766", "generic_name": "Galantamine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Galantamine", "active_ingredients": [{"name": "GALANTAMINE HYDROBROMIDE", "strength": "4 mg/1"}], "application_number": "ANDA090957", "marketing_category": "ANDA", "marketing_start_date": "20110329", "listing_expiration_date": "20261231"}