zolmitriptan

Generic: zolmitriptan

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name zolmitriptan
Generic Name zolmitriptan
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

zolmitriptan 5 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-915
Product ID 65862-915_3c989433-86b6-4155-b2b0-156724df45df
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207021
Listing Expiration 2026-12-31
Marketing Start 2016-05-11

Pharmacologic Class

Established (EPC)
serotonin-1b and serotonin-1d receptor agonist [epc]
Mechanism of Action
serotonin 1b receptor agonists [moa] serotonin 1d receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65862915
Hyphenated Format 65862-915

Supplemental Identifiers

RxCUI
200193 200194
UPC
0365862914699
UNII
2FS66TH3YW
NUI
N0000175763 N0000175764 N0000175765

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 zolmitriptan (source: ndc)
Generic Name zolmitriptan (source: ndc)
Application Number ANDA207021 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (65862-915-64) / 3 TABLET, FILM COATED in 1 BLISTER PACK (65862-915-03)
source: ndc

Packages (1)

65862-915-64 1 BLISTER PACK in 1 CARTON (65862-915-64) / 3 TABLET, FILM COATED in 1 BLISTER PACK (65862-915-03)

Ingredients (1)

zolmitriptan (5 mg/1)

Linked Drug Pages (1)

Zolmitriptan ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3c989433-86b6-4155-b2b0-156724df45df", "openfda": {"nui": ["N0000175763", "N0000175764", "N0000175765"], "upc": ["0365862914699"], "unii": ["2FS66TH3YW"], "rxcui": ["200193", "200194"], "spl_set_id": ["9212b076-b1ae-4c06-bd56-0ae3c5c9acdf"], "pharm_class_epc": ["Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "pharm_class_moa": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (65862-915-64)  / 3 TABLET, FILM COATED in 1 BLISTER PACK (65862-915-03)", "package_ndc": "65862-915-64", "marketing_start_date": "20160511"}], "brand_name": "Zolmitriptan", "product_id": "65862-915_3c989433-86b6-4155-b2b0-156724df45df", "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": "65862-915", "generic_name": "Zolmitriptan", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zolmitriptan", "active_ingredients": [{"name": "ZOLMITRIPTAN", "strength": "5 mg/1"}], "application_number": "ANDA207021", "marketing_category": "ANDA", "marketing_start_date": "20160511", "listing_expiration_date": "20261231"}