sumatriptan succinate

Generic: sumatriptan succinate

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sumatriptan succinate
Generic Name sumatriptan succinate
Labeler direct_rx
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sumatriptan succinate 50 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-433
Product ID 72189-433_2c4d7d0d-6552-336d-e063-6294a90a0ea4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078295
Listing Expiration 2026-12-31
Marketing Start 2023-03-13

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 72189433
Hyphenated Format 72189-433

Supplemental Identifiers

RxCUI
313161
UNII
J8BDZ68989

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
  • 9 TABLET, FILM COATED in 1 BOTTLE (72189-433-09)
source: ndc

Packages (1)

72189-433-09 9 TABLET, FILM COATED in 1 BOTTLE (72189-433-09)

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": "2c4d7d0d-6552-336d-e063-6294a90a0ea4", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313161"], "spl_set_id": ["f6c907a3-9624-f893-e053-6294a90a31af"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET, FILM COATED in 1 BOTTLE (72189-433-09)", "package_ndc": "72189-433-09", "marketing_start_date": "20230313"}], "brand_name": "Sumatriptan Succinate", "product_id": "72189-433_2c4d7d0d-6552-336d-e063-6294a90a0ea4", "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": "72189-433", "generic_name": "Sumatriptan Succinate", "labeler_name": "Direct_Rx", "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": "20230313", "listing_expiration_date": "20261231"}