galantamine

Generic: galantamine

Labeler: slate run pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name galantamine
Generic Name galantamine
Labeler slate run pharmaceuticals, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

galantamine hydrobromide 8 mg/1

Manufacturer
Slate Run Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 70436-005
Product ID 70436-005_4685d03a-2fae-235e-e063-6394a90afd77
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077604
Listing Expiration 2026-12-31
Marketing Start 2017-08-02

Pharmacologic Class

Classes
cholinesterase inhibitor [epc] cholinesterase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70436005
Hyphenated Format 70436-005

Supplemental Identifiers

RxCUI
310436 310437 579148
UPC
0370436006069 0370436004065 0370436005062
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 (70436-005-06)
source: ndc

Packages (1)

70436-005-06 60 TABLET, FILM COATED in 1 BOTTLE (70436-005-06)

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": "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 (70436-005-06)", "package_ndc": "70436-005-06", "marketing_start_date": "20170802"}], "brand_name": "Galantamine", "product_id": "70436-005_4685d03a-2fae-235e-e063-6394a90afd77", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "70436-005", "generic_name": "galantamine", "labeler_name": "Slate Run Pharmaceuticals, 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": "20170802", "listing_expiration_date": "20261231"}