galantamine

Generic: galantamine

Labeler: upsher-smith laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name galantamine
Generic Name galantamine
Labeler upsher-smith laboratories, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

galantamine hydrobromide 8 mg/1

Manufacturer
Upsher-Smith Laboratories, LLC

Identifiers & Regulatory

Product NDC 24979-723
Product ID 24979-723_4685d63a-b3bc-416d-e063-6294a90afce3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077604
Listing Expiration 2026-12-31
Marketing Start 2024-03-06

Pharmacologic Class

Classes
cholinesterase inhibitor [epc] cholinesterase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 24979723
Hyphenated Format 24979-723

Supplemental Identifiers

RxCUI
310436 310437 579148
UPC
0324979724041 0324979723044 0324979722047
UNII
MJ4PTD2VVW

Packaging Origin

Original Packager
true

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 8 mg/1
source: ndc
Packaging
  • 60 TABLET, FILM COATED in 1 BOTTLE (24979-723-04)
source: ndc

Packages (1)

24979-723-04 60 TABLET, FILM COATED in 1 BOTTLE (24979-723-04)

Ingredients (1)

galantamine hydrobromide (8 mg/1)

Linked Drug Pages (1)

Galantamine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4685d63a-b3bc-416d-e063-6294a90afce3", "openfda": {"upc": ["0324979724041", "0324979723044", "0324979722047"], "unii": ["MJ4PTD2VVW"], "rxcui": ["310436", "310437", "579148"], "spl_set_id": ["10497273-d907-0514-e063-6294a90a1362"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (24979-723-04)", "package_ndc": "24979-723-04", "marketing_start_date": "20240306"}], "brand_name": "Galantamine", "product_id": "24979-723_4685d63a-b3bc-416d-e063-6294a90afce3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "24979-723", "generic_name": "galantamine", "labeler_name": "Upsher-Smith Laboratories, LLC", "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": "20240306", "listing_expiration_date": "20261231"}