sumatriptan succinate

Generic: sumatriptan succinate

Labeler: mylan pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sumatriptan succinate
Generic Name sumatriptan succinate
Labeler mylan pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

sumatriptan succinate 100 mg/1

Manufacturer
Mylan Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 0378-5632
Product ID 0378-5632_cd918be8-d6c0-4dcc-aa7d-32bd7017fa1d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077744
Listing Expiration 2027-12-31
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 03785632
Hyphenated Format 0378-5632

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 succinate (source: ndc)
Generic Name sumatriptan succinate (source: ndc)
Application Number ANDA077744 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5632-59)
source: ndc

Packages (1)

0378-5632-59 9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5632-59)

Ingredients (1)

sumatriptan succinate (100 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": "cd918be8-d6c0-4dcc-aa7d-32bd7017fa1d", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313160", "313161", "315223"], "spl_set_id": ["1d2cd01c-05e7-44cf-a71d-0f474e826b7e"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5632-59)", "package_ndc": "0378-5632-59", "marketing_start_date": "20090810"}], "brand_name": "Sumatriptan Succinate", "product_id": "0378-5632_cd918be8-d6c0-4dcc-aa7d-32bd7017fa1d", "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": "0378-5632", "generic_name": "sumatriptan succinate", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sumatriptan Succinate", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA077744", "marketing_category": "ANDA", "marketing_start_date": "20090810", "listing_expiration_date": "20271231"}