sumatriptan

Generic: sumatriptan

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

Drug Facts

Product Profile

Brand Name sumatriptan
Generic Name sumatriptan
Labeler hikma pharmaceuticals usa inc.
Dosage Form INJECTION
Routes
SUBCUTANEOUS
Active Ingredients

sumatriptan succinate 6 mg/.5mL

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9638
Product ID 0143-9638_38f8761d-784e-407e-9dda-73fd78a829f4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200183
Listing Expiration 2026-12-31
Marketing Start 2013-09-16

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 01439638
Hyphenated Format 0143-9638

Supplemental Identifiers

RxCUI
313165
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 ANDA200183 (source: ndc)
Routes
SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 6 mg/.5mL
source: ndc
Packaging
  • 5 VIAL in 1 CARTON (0143-9638-05) / .5 mL in 1 VIAL (0143-9638-01)
  • 25 VIAL in 1 CARTON (0143-9638-25) / .5 mL in 1 VIAL (0143-9638-01)
source: ndc

Packages (2)

Ingredients (1)

sumatriptan succinate (6 mg/.5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "38f8761d-784e-407e-9dda-73fd78a829f4", "openfda": {"unii": ["J8BDZ68989"], "rxcui": ["313165"], "spl_set_id": ["2b417f8c-9e5b-45a1-b8af-183818258df9"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL in 1 CARTON (0143-9638-05)  / .5 mL in 1 VIAL (0143-9638-01)", "package_ndc": "0143-9638-05", "marketing_start_date": "20130916"}, {"sample": false, "description": "25 VIAL in 1 CARTON (0143-9638-25)  / .5 mL in 1 VIAL (0143-9638-01)", "package_ndc": "0143-9638-25", "marketing_start_date": "20130916"}], "brand_name": "SUMATRIPTAN", "product_id": "0143-9638_38f8761d-784e-407e-9dda-73fd78a829f4", "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": "0143-9638", "generic_name": "sumatriptan", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SUMATRIPTAN", "active_ingredients": [{"name": "SUMATRIPTAN SUCCINATE", "strength": "6 mg/.5mL"}], "application_number": "ANDA200183", "marketing_category": "ANDA", "marketing_start_date": "20130916", "listing_expiration_date": "20261231"}