sumatriptan

Generic: sumatriptan

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sumatriptan
Generic Name sumatriptan
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sumatriptan succinate 25 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7436
Product ID 50090-7436_6a1a0b16-097b-47c2-aa32-01916f7df946
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078284
Listing Expiration 2026-12-31
Marketing Start 2022-02-18

Pharmacologic Class

Classes
serotonin 1b receptor agonists [moa] serotonin 1d receptor agonists [moa] serotonin-1b and serotonin-1d receptor agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907436
Hyphenated Format 50090-7436

Supplemental Identifiers

RxCUI
315223
UNII
J8BDZ68989

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 sumatriptan (source: ndc)
Generic Name sumatriptan (source: ndc)
Application Number ANDA078284 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (50090-7436-0) / 9 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (1)

50090-7436-0 1 BLISTER PACK in 1 CARTON (50090-7436-0) / 9 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

sumatriptan succinate (25 mg/1)

Linked Drug Pages (1)

Sumatriptan ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6a1a0b16-097b-47c2-aa32-01916f7df946", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["315223"], "spl_set_id": ["790acc89-81b3-4869-92e7-dc9f7fa6567b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50090-7436-0)  / 9 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "50090-7436-0", "marketing_start_date": "20241106"}], "brand_name": "Sumatriptan", "product_id": "50090-7436_6a1a0b16-097b-47c2-aa32-01916f7df946", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "50090-7436", "generic_name": "Sumatriptan", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "25 mg/1"}], "application_number": "ANDA078284", "marketing_category": "ANDA", "marketing_start_date": "20220218", "listing_expiration_date": "20261231"}