naratriptan

Generic: naratriptan

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naratriptan
Generic Name naratriptan
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

naratriptan hydrochloride 1 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-054
Product ID 23155-054_61e37b1d-f036-4c35-9073-ce456efd8007
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200502
Listing Expiration 2026-12-31
Marketing Start 2011-03-15

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 23155054
Hyphenated Format 23155-054

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 ANDA200502 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (23155-054-03)
  • 500 TABLET in 1 BOTTLE (23155-054-05)
  • 9 TABLET in 1 BLISTER PACK (23155-054-19)
source: ndc

Packages (3)

23155-054-03 30 TABLET in 1 BOTTLE (23155-054-03) 23155-054-05 500 TABLET in 1 BOTTLE (23155-054-05) 23155-054-19 9 TABLET in 1 BLISTER PACK (23155-054-19)

Ingredients (1)

naratriptan hydrochloride (1 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": "61e37b1d-f036-4c35-9073-ce456efd8007", "openfda": {"unii": ["10X8X4P12Z"], "rxcui": ["311918", "314135"], "spl_set_id": ["41c29652-32f8-48dc-9038-0e2195aa2084"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (23155-054-03)", "package_ndc": "23155-054-03", "marketing_start_date": "20110315"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-054-05)", "package_ndc": "23155-054-05", "marketing_start_date": "20110315"}, {"sample": false, "description": "9 TABLET in 1 BLISTER PACK (23155-054-19)", "package_ndc": "23155-054-19", "marketing_start_date": "20110315"}], "brand_name": "naratriptan", "product_id": "23155-054_61e37b1d-f036-4c35-9073-ce456efd8007", "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": "23155-054", "generic_name": "naratriptan", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "naratriptan", "active_ingredients": [{"name": "NARATRIPTAN HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA200502", "marketing_category": "ANDA", "marketing_start_date": "20110315", "listing_expiration_date": "20261231"}