sumatriptan

Generic: sumatriptan succinate

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sumatriptan
Generic Name sumatriptan succinate
Labeler asclemed usa, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sumatriptan succinate 100 mg/1

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-500
Product ID 76420-500_eacf382a-98ac-e3ad-e053-2995a90a44e8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078327
Listing Expiration 2026-12-31
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 76420500
Hyphenated Format 76420-500

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
  • 9 TABLET in 1 BLISTER PACK (76420-500-09)
source: ndc

Packages (1)

76420-500-09 9 TABLET in 1 BLISTER PACK (76420-500-09)

Ingredients (1)

sumatriptan succinate (100 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": "eacf382a-98ac-e3ad-e053-2995a90a44e8", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313160", "313161", "315223"], "spl_set_id": ["77f9f135-e840-48f0-81e8-73e08433e768"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET in 1 BLISTER PACK (76420-500-09)", "package_ndc": "76420-500-09", "marketing_start_date": "20221012"}], "brand_name": "Sumatriptan", "product_id": "76420-500_eacf382a-98ac-e3ad-e053-2995a90a44e8", "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": "76420-500", "generic_name": "Sumatriptan Succinate", "labeler_name": "Asclemed USA, Inc.", "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": "20261231"}