naratriptan

Generic: naratriptan

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

Drug Facts

Product Profile

Brand Name naratriptan
Generic Name naratriptan
Labeler hikma pharmaceuticals usa inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

naratriptan hydrochloride 2.5 mg/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0054-0279
Product ID 0054-0279_14eeba7d-700d-4ac1-a71e-d6a1fca8aaab
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090381
Listing Expiration 2026-12-31
Marketing Start 2010-07-07

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 00540279
Hyphenated Format 0054-0279

Supplemental Identifiers

RxCUI
311918 314135
UNII
10X8X4P12Z

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 naratriptan (source: ndc)
Generic Name naratriptan (source: ndc)
Application Number ANDA090381 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/1
source: ndc
Packaging
  • 9 TABLET in 1 BOTTLE (0054-0279-03)
source: ndc

Packages (1)

0054-0279-03 9 TABLET in 1 BOTTLE (0054-0279-03)

Ingredients (1)

naratriptan hydrochloride (2.5 mg/1)

Linked Drug Pages (1)

Naratriptan ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "14eeba7d-700d-4ac1-a71e-d6a1fca8aaab", "openfda": {"unii": ["10X8X4P12Z"], "rxcui": ["311918", "314135"], "spl_set_id": ["fd1944b3-8054-4faa-a82e-d818dfdd3875"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "9 TABLET in 1 BOTTLE (0054-0279-03)", "package_ndc": "0054-0279-03", "marketing_start_date": "20101007"}], "brand_name": "Naratriptan", "product_id": "0054-0279_14eeba7d-700d-4ac1-a71e-d6a1fca8aaab", "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": "0054-0279", "generic_name": "Naratriptan", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naratriptan", "active_ingredients": [{"name": "NARATRIPTAN HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA090381", "marketing_category": "ANDA", "marketing_start_date": "20100707", "listing_expiration_date": "20261231"}