sumatriptan

Generic: sumatriptan succinate

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

Drug Facts

Product Profile

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

sumatriptan succinate 100 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1130
Product ID 50090-1130_600695df-cc8b-40cd-83ec-b8f651f2c163
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078327
Listing Expiration 2027-12-31
Marketing Start 2009-08-17

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 500901130
Hyphenated Format 50090-1130

Supplemental Identifiers

RxCUI
313160 313161 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 succinate (source: ndc)
Application Number ANDA078327 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (50090-1130-0) / 9 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

sumatriptan succinate (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "600695df-cc8b-40cd-83ec-b8f651f2c163", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313160", "313161", "315223"], "spl_set_id": ["62ba6fef-467a-4500-993c-51907f12a67c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50090-1130-0)  / 9 TABLET in 1 BLISTER PACK", "package_ndc": "50090-1130-0", "marketing_start_date": "20141128"}], "brand_name": "Sumatriptan", "product_id": "50090-1130_600695df-cc8b-40cd-83ec-b8f651f2c163", "dosage_form": "TABLET", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "50090-1130", "generic_name": "Sumatriptan Succinate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA078327", "marketing_category": "ANDA", "marketing_start_date": "20090817", "listing_expiration_date": "20271231"}