Package 70436-006-06

Brand: galantamine

Generic: galantamine
NDC Package

Package Facts

Identity

Package NDC 70436-006-06
Digits Only 7043600606
Product NDC 70436-006
Product ID 70436-006_4685d03a-2fae-235e-e063-6394a90afd77
Description

60 TABLET, FILM COATED in 1 BOTTLE (70436-006-06)

Marketing

Marketing Status
Marketed Since 2017-08-02
Brand galantamine
Generic galantamine
Sample Package No

Linked Drug Pages (1)

Galantamine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4685d03a-2fae-235e-e063-6394a90afd77", "openfda": {"upc": ["0370436006069", "0370436004065", "0370436005062"], "unii": ["MJ4PTD2VVW"], "rxcui": ["310436", "310437", "579148"], "spl_set_id": ["56f365e5-0a23-4f69-e054-00144ff8d46c"], "manufacturer_name": ["Slate Run Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (70436-006-06)", "package_ndc": "70436-006-06", "marketing_start_date": "20170802"}], "brand_name": "Galantamine", "product_id": "70436-006_4685d03a-2fae-235e-e063-6394a90afd77", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "70436-006", "generic_name": "galantamine", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Galantamine", "active_ingredients": [{"name": "GALANTAMINE HYDROBROMIDE", "strength": "12 mg/1"}], "application_number": "ANDA077604", "marketing_category": "ANDA", "marketing_start_date": "20170802", "listing_expiration_date": "20261231"}