eletriptan hbr

Generic: eletriptan hbr

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name eletriptan hbr
Generic Name eletriptan hbr
Labeler direct_rx
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

eletriptan hydrobromide 40 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-517
Product ID 72189-517_2c4e7a35-ff54-4971-e063-6294a90ae9df
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210708
Listing Expiration 2026-12-31
Marketing Start 2023-10-11

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 72189517
Hyphenated Format 72189-517

Supplemental Identifiers

RxCUI
359494
UNII
M41W832TA3

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 eletriptan hbr (source: ndc)
Generic Name eletriptan hbr (source: ndc)
Application Number ANDA210708 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 6 TABLET, FILM COATED in 1 CARTON (72189-517-06)
source: ndc

Packages (1)

Ingredients (1)

eletriptan hydrobromide (40 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c4e7a35-ff54-4971-e063-6294a90ae9df", "openfda": {"unii": ["M41W832TA3"], "rxcui": ["359494"], "spl_set_id": ["077134d1-427d-6235-e063-6394a90abcf6"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 CARTON (72189-517-06)", "package_ndc": "72189-517-06", "marketing_start_date": "20231011"}], "brand_name": "Eletriptan HBR", "product_id": "72189-517_2c4e7a35-ff54-4971-e063-6294a90ae9df", "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": "72189-517", "generic_name": "Eletriptan HBR", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Eletriptan HBR", "active_ingredients": [{"name": "ELETRIPTAN HYDROBROMIDE", "strength": "40 mg/1"}], "application_number": "ANDA210708", "marketing_category": "ANDA", "marketing_start_date": "20231011", "listing_expiration_date": "20261231"}