Package 57237-049-60
Brand: galantamine
Generic: galantaminePackage Facts
Identity
Package NDC
57237-049-60
Digits Only
5723704960
Product NDC
57237-049
Description
60 TABLET, FILM COATED in 1 BOTTLE (57237-049-60)
Marketing
Marketing Status
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": "f59a93d6-9a01-40ad-a9ef-4eaacff23b79", "openfda": {"unii": ["MJ4PTD2VVW"], "rxcui": ["310436", "310437", "579148"], "spl_set_id": ["a0dc1a93-b7b8-4179-8ea7-ceecbe1ef243"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (57237-049-60)", "package_ndc": "57237-049-60", "marketing_start_date": "20110329"}], "brand_name": "Galantamine", "product_id": "57237-049_f59a93d6-9a01-40ad-a9ef-4eaacff23b79", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "57237-049", "generic_name": "Galantamine", "labeler_name": "Rising Pharma Holdings, Inc.", "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"}