sumatriptan succinate

Generic: sumatriptan succinate

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

Drug Facts

Product Profile

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

sumatriptan succinate 50 mg/1

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-093
Product ID 76420-093_b26ec84b-1af1-b04d-e053-2a95a90a8c78
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076847
Listing Expiration 2026-12-31
Marketing Start 2009-11-17

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 76420093
Hyphenated Format 76420-093

Supplemental Identifiers

RxCUI
313161
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 succinate (source: ndc)
Generic Name sumatriptan succinate (source: ndc)
Application Number ANDA076847 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 9 BLISTER PACK in 1 CARTON (76420-093-09) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

sumatriptan succinate (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b26ec84b-1af1-b04d-e053-2a95a90a8c78", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313161"], "spl_set_id": ["b16886d0-224b-4d83-85c4-bc3eb3606c17"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "9 BLISTER PACK in 1 CARTON (76420-093-09)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "76420-093-09", "marketing_start_date": "20201024"}], "brand_name": "Sumatriptan Succinate", "product_id": "76420-093_b26ec84b-1af1-b04d-e053-2a95a90a8c78", "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": "76420-093", "generic_name": "Sumatriptan Succinate", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan Succinate", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "50 mg/1"}], "application_number": "ANDA076847", "marketing_category": "ANDA", "marketing_start_date": "20091117", "listing_expiration_date": "20261231"}