sumatriptan

Generic: sumatriptan

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

Drug Facts

Product Profile

Brand Name sumatriptan
Generic Name sumatriptan
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sumatriptan succinate 100 mg/1

Manufacturer
SUN PHARMACEUTICAL INDUSTRIES, INC.

Identifiers & Regulatory

Product NDC 63304-099
Product ID 63304-099_9bc4f2da-41f0-42e2-98b2-b689c02d0a3e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076572
Listing Expiration 2026-12-31
Marketing Start 2009-02-10

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 63304099
Hyphenated Format 63304-099

Supplemental Identifiers

RxCUI
313160 313161 315223
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 (source: ndc)
Application Number ANDA076572 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 120 TABLET in 1 BOTTLE (63304-099-13)
  • 1 BLISTER PACK in 1 CARTON (63304-099-19) / 9 TABLET in 1 BLISTER PACK
  • 5 TABLET in 1 BOTTLE (63304-099-45)
source: ndc

Packages (3)

63304-099-13 120 TABLET in 1 BOTTLE (63304-099-13) 63304-099-19 1 BLISTER PACK in 1 CARTON (63304-099-19) / 9 TABLET in 1 BLISTER PACK 63304-099-45 5 TABLET in 1 BOTTLE (63304-099-45)

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": "9bc4f2da-41f0-42e2-98b2-b689c02d0a3e", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313160", "313161", "315223"], "spl_set_id": ["c87cf537-9f7f-400e-ac4b-86e6f7e78775"], "manufacturer_name": ["SUN PHARMACEUTICAL INDUSTRIES, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (63304-099-13)", "package_ndc": "63304-099-13", "marketing_start_date": "20090210"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (63304-099-19)  / 9 TABLET in 1 BLISTER PACK", "package_ndc": "63304-099-19", "marketing_start_date": "20090210"}, {"sample": false, "description": "5 TABLET in 1 BOTTLE (63304-099-45)", "package_ndc": "63304-099-45", "marketing_start_date": "20090210"}], "brand_name": "Sumatriptan", "product_id": "63304-099_9bc4f2da-41f0-42e2-98b2-b689c02d0a3e", "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": "63304-099", "generic_name": "Sumatriptan", "labeler_name": "SUN PHARMACEUTICAL INDUSTRIES, INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA076572", "marketing_category": "ANDA", "marketing_start_date": "20090210", "listing_expiration_date": "20261231"}