galantamine
Generic: galantamine
Labeler: golden state medical supply, inc.Drug Facts
Product Profile
Brand Name
galantamine
Generic Name
galantamine
Labeler
golden state medical supply, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
galantamine hydrobromide 12 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51407-908
Product ID
51407-908_48c63678-9fd2-5b7e-e063-6294a90ae51d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077604
Listing Expiration
2027-12-31
Marketing Start
2009-02-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51407908
Hyphenated Format
51407-908
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
galantamine (source: ndc)
Generic Name
galantamine (source: ndc)
Application Number
ANDA077604 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 12 mg/1
Packaging
- 60 TABLET, FILM COATED in 1 BOTTLE (51407-908-60)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48c63678-9fd2-5b7e-e063-6294a90ae51d", "openfda": {"unii": ["MJ4PTD2VVW"], "rxcui": ["310436", "310437", "579148"], "spl_set_id": ["18fd8860-d9ab-1b17-e063-6294a90aad9a"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (51407-908-60)", "package_ndc": "51407-908-60", "marketing_start_date": "20240415"}], "brand_name": "Galantamine", "product_id": "51407-908_48c63678-9fd2-5b7e-e063-6294a90ae51d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "51407-908", "generic_name": "galantamine", "labeler_name": "Golden State Medical Supply, Inc.", "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": "20090206", "listing_expiration_date": "20271231"}