Package 0054-0137-49

Brand: galantamine hydrobromide

Generic: galantamine hydrobromide
NDC Package

Package Facts

Identity

Package NDC 0054-0137-49
Digits Only 0054013749
Product NDC 0054-0137
Product ID 0054-0137_b2bf3efc-7521-4ff7-b77c-6e312e34b3c4
Description

100 mL in 1 BOTTLE (0054-0137-49)

Marketing

Marketing Status
Marketed Since 2009-08-14
Brand galantamine hydrobromide
Generic galantamine hydrobromide
Sample Package No

Linked Drug Pages (1)

Galantamine Hydrobromide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b2bf3efc-7521-4ff7-b77c-6e312e34b3c4", "openfda": {"unii": ["MJ4PTD2VVW"], "rxcui": ["860901"], "spl_set_id": ["d5b0e225-e94d-4324-afb2-b6e51c949dd0"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (0054-0137-49)", "package_ndc": "0054-0137-49", "marketing_start_date": "20090814"}], "brand_name": "Galantamine Hydrobromide", "product_id": "0054-0137_b2bf3efc-7521-4ff7-b77c-6e312e34b3c4", "dosage_form": "SOLUTION", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "0054-0137", "generic_name": "Galantamine Hydrobromide", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Galantamine Hydrobromide", "active_ingredients": [{"name": "GALANTAMINE HYDROBROMIDE", "strength": "4 mg/mL"}], "application_number": "ANDA078185", "marketing_category": "ANDA", "marketing_start_date": "20090814", "listing_expiration_date": "20261231"}