sumatriptan
Generic: sumatriptan succinate
Labeler: xellia pharmaceuticals usa llcDrug Facts
Product Profile
Brand Name
sumatriptan
Generic Name
sumatriptan succinate
Labeler
xellia pharmaceuticals usa llc
Dosage Form
INJECTION
Routes
Active Ingredients
sumatriptan succinate 6 mg/.5mL
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70594068
Hyphenated Format
70594-068
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 6 mg/.5mL
Packaging
- 5 VIAL in 1 CARTON (70594-068-02) / .5 mL in 1 VIAL (70594-068-01)
Packages (1)
Ingredients (1)
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"}