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 TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sumatriptan succinate 50 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 62756-521
Product ID 62756-521_9035f04f-b353-4883-9ac2-e030f18bfc1c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078295
Listing Expiration 2026-12-31
Marketing Start 2009-08-10

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 62756521
Hyphenated Format 62756-521

Supplemental Identifiers

UPC
0362756521889 0362756522886
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 ANDA078295 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 3 BLISTER PACK in 1 CARTON (62756-521-01) / 9 TABLET, FILM COATED in 1 BLISTER PACK
  • 100 TABLET, FILM COATED in 1 BOTTLE (62756-521-08)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (62756-521-18)
  • 9 BLISTER PACK in 1 CARTON (62756-521-69) / 1 TABLET, FILM COATED in 1 BLISTER PACK
  • 30 TABLET, FILM COATED in 1 BOTTLE (62756-521-83)
  • 100 TABLET, FILM COATED in 1 BOTTLE (62756-521-88)
  • 9 BLISTER PACK in 1 CARTON (62756-521-93) / 1 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (7)

62756-521-01 3 BLISTER PACK in 1 CARTON (62756-521-01) / 9 TABLET, FILM COATED in 1 BLISTER PACK 62756-521-08 100 TABLET, FILM COATED in 1 BOTTLE (62756-521-08) 62756-521-18 1000 TABLET, FILM COATED in 1 BOTTLE (62756-521-18) 62756-521-69 9 BLISTER PACK in 1 CARTON (62756-521-69) / 1 TABLET, FILM COATED in 1 BLISTER PACK 62756-521-83 30 TABLET, FILM COATED in 1 BOTTLE (62756-521-83) 62756-521-88 100 TABLET, FILM COATED in 1 BOTTLE (62756-521-88) 62756-521-93 9 BLISTER PACK in 1 CARTON (62756-521-93) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

sumatriptan succinate (50 mg/1)

Linked Drug Pages (1)

sumatriptan succinate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9035f04f-b353-4883-9ac2-e030f18bfc1c", "openfda": {"upc": ["0362756521889", "0362756522886"], "unii": ["J8BDZ68989"], "spl_set_id": ["9485cc30-15e8-4b53-876d-db317145474b"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (62756-521-01)  / 9 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "62756-521-01", "marketing_start_date": "20201101"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62756-521-08)", "package_ndc": "62756-521-08", "marketing_start_date": "20090810"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62756-521-18)", "package_ndc": "62756-521-18", "marketing_start_date": "20090810"}, {"sample": false, "description": "9 BLISTER PACK in 1 CARTON (62756-521-69)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "62756-521-69", "marketing_start_date": "20090810"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62756-521-83)", "package_ndc": "62756-521-83", "marketing_start_date": "20090810"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62756-521-88)", "package_ndc": "62756-521-88", "marketing_start_date": "20090810"}, {"sample": false, "description": "9 BLISTER PACK in 1 CARTON (62756-521-93)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "62756-521-93", "marketing_start_date": "20090810"}], "brand_name": "sumatriptan succinate", "product_id": "62756-521_9035f04f-b353-4883-9ac2-e030f18bfc1c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "62756-521", "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": "50 mg/1"}], "application_number": "ANDA078295", "marketing_category": "ANDA", "marketing_start_date": "20090810", "listing_expiration_date": "20261231"}