Package 65862-459-99

Brand: galantamine

Generic: galantamine
NDC Package

Package Facts

Identity

Package NDC 65862-459-99
Digits Only 6586245999
Product NDC 65862-459
Description

1000 TABLET, FILM COATED in 1 BOTTLE (65862-459-99)

Marketing

Marketing Status
Marketed Since 2011-03-29
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": "a5420811-7ce9-4ea6-8d93-6422f016b0d8", "openfda": {"upc": ["0365862460608"], "unii": ["MJ4PTD2VVW"], "rxcui": ["310436", "310437", "579148"], "spl_set_id": ["4e05d1da-0eb8-4fe0-8259-f1ebb170e0dc"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (65862-459-60)", "package_ndc": "65862-459-60", "marketing_start_date": "20110329"}, {"sample": false, "description": "7000 TABLET, FILM COATED in 1 BOTTLE (65862-459-71)", "package_ndc": "65862-459-71", "marketing_start_date": "20110329"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-459-99)", "package_ndc": "65862-459-99", "marketing_start_date": "20110329"}], "brand_name": "Galantamine", "product_id": "65862-459_a5420811-7ce9-4ea6-8d93-6422f016b0d8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "65862-459", "generic_name": "Galantamine", "labeler_name": "Aurobindo Pharma Limited", "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"}