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 8 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
51407-907
Product ID
51407-907_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
51407907
Hyphenated Format
51407-907
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
- 8 mg/1
Packaging
- 60 TABLET, FILM COATED in 1 BOTTLE (51407-907-60)
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 (51407-907-60)", "package_ndc": "51407-907-60", "marketing_start_date": "20240415"}], "brand_name": "Galantamine", "product_id": "51407-907_48c63678-9fd2-5b7e-e063-6294a90ae51d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "51407-907", "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": "8 mg/1"}], "application_number": "ANDA077604", "marketing_category": "ANDA", "marketing_start_date": "20090206", "listing_expiration_date": "20271231"}