sumatriptan

Generic: sumatriptan succinate

Labeler: xellia pharmaceuticals usa llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sumatriptan
Generic Name sumatriptan succinate
Labeler xellia pharmaceuticals usa llc
Dosage Form INJECTION
Routes
SUBCUTANEOUS
Active Ingredients

sumatriptan succinate 6 mg/.5mL

Manufacturer
Xellia Pharmaceuticals USA LLC

Identifiers & Regulatory

Product NDC 70594-068
Product ID 70594-068_44ed271d-bc7e-48f7-bb63-0ecdb70fdad4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213998
Listing Expiration 2026-12-31
Marketing Start 2022-01-01

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 70594068
Hyphenated Format 70594-068

Supplemental Identifiers

RxCUI
313165
UNII
J8BDZ68989

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 sumatriptan (source: ndc)
Generic Name sumatriptan succinate (source: ndc)
Application Number ANDA213998 (source: ndc)
Routes
SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 6 mg/.5mL
source: ndc
Packaging
  • 5 VIAL in 1 CARTON (70594-068-02) / .5 mL in 1 VIAL (70594-068-01)
source: ndc

Packages (1)

Ingredients (1)

sumatriptan succinate (6 mg/.5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "44ed271d-bc7e-48f7-bb63-0ecdb70fdad4", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313165"], "spl_set_id": ["f42c6e00-e693-48f3-8e84-c3f139e1adf5"], "manufacturer_name": ["Xellia Pharmaceuticals USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL in 1 CARTON (70594-068-02)  / .5 mL in 1 VIAL (70594-068-01)", "package_ndc": "70594-068-02", "marketing_start_date": "20220101"}], "brand_name": "Sumatriptan", "product_id": "70594-068_44ed271d-bc7e-48f7-bb63-0ecdb70fdad4", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "70594-068", "generic_name": "SUMATRIPTAN SUCCINATE", "labeler_name": "Xellia Pharmaceuticals USA LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "6 mg/.5mL"}], "application_number": "ANDA213998", "marketing_category": "ANDA", "marketing_start_date": "20220101", "listing_expiration_date": "20261231"}