sumatriptan succinate

Generic: sumatriptan succinate

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sumatriptan succinate
Generic Name sumatriptan succinate
Labeler sun pharmaceutical industries, inc.
Dosage Form INJECTION
Routes
SUBCUTANEOUS
Active Ingredients

sumatriptan succinate 6 mg/.5mL

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 47335-276
Product ID 47335-276_2642fcb9-4170-4b4c-818b-74c071cb567e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090358
Listing Expiration 2027-12-31
Marketing Start 2025-08-20

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 47335276
Hyphenated Format 47335-276

Supplemental Identifiers

RxCUI
1657151
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 succinate (source: ndc)
Generic Name sumatriptan succinate (source: ndc)
Application Number ANDA090358 (source: ndc)
Routes
SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 6 mg/.5mL
source: ndc
Packaging
  • 1 SYRINGE in 1 PACKAGE (47335-276-40) / .5 mL in 1 SYRINGE
  • 2 SYRINGE in 1 PACKAGE (47335-276-41) / .5 mL in 1 SYRINGE
source: ndc

Packages (2)

47335-276-40 1 SYRINGE in 1 PACKAGE (47335-276-40) / .5 mL in 1 SYRINGE 47335-276-41 2 SYRINGE in 1 PACKAGE (47335-276-41) / .5 mL in 1 SYRINGE

Ingredients (1)

sumatriptan succinate (6 mg/.5mL)

Linked Drug Pages (1)

Sumatriptan Succinate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBCUTANEOUS"], "spl_id": "2642fcb9-4170-4b4c-818b-74c071cb567e", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["1657151"], "spl_set_id": ["f235152e-dd8d-4679-9d9f-404fe5ff4fba"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE in 1 PACKAGE (47335-276-40)  / .5 mL in 1 SYRINGE", "package_ndc": "47335-276-40", "marketing_start_date": "20250820"}, {"sample": false, "description": "2 SYRINGE in 1 PACKAGE (47335-276-41)  / .5 mL in 1 SYRINGE", "package_ndc": "47335-276-41", "marketing_start_date": "20250820"}], "brand_name": "Sumatriptan Succinate", "product_id": "47335-276_2642fcb9-4170-4b4c-818b-74c071cb567e", "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": "47335-276", "generic_name": "Sumatriptan Succinate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan Succinate", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "6 mg/.5mL"}], "application_number": "ANDA090358", "marketing_category": "ANDA", "marketing_start_date": "20250820", "listing_expiration_date": "20271231"}