ondansetron odt

Generic: ondansetron

Labeler: advanced rx of tennessee, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ondansetron odt
Generic Name ondansetron
Labeler advanced rx of tennessee, llc
Dosage Form TABLET, ORALLY DISINTEGRATING
Routes
ORAL
Active Ingredients

ondansetron 4 mg/1

Manufacturer
Advanced Rx of Tennessee, LLC

Identifiers & Regulatory

Product NDC 80425-0073
Product ID 80425-0073_2a98d9c1-b777-40b1-e063-6294a90a20e4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090469
Listing Expiration 2026-12-31
Marketing Start 2010-04-12

Pharmacologic Class

Established (EPC)
serotonin-3 receptor antagonist [epc]
Mechanism of Action
serotonin 3 receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 804250073
Hyphenated Format 80425-0073

Supplemental Identifiers

RxCUI
104894
UNII
4AF302ESOS
NUI
N0000175817 N0000175818

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 ondansetron odt (source: ndc)
Generic Name ondansetron (source: ndc)
Application Number ANDA090469 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 20 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (80425-0073-1)
  • 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (80425-0073-2)
source: ndc

Packages (2)

80425-0073-1 20 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (80425-0073-1) 80425-0073-2 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (80425-0073-2)

Ingredients (1)

ondansetron (4 mg/1)

Linked Drug Pages (1)

Ondansetron ODT ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a98d9c1-b777-40b1-e063-6294a90a20e4", "openfda": {"nui": ["N0000175817", "N0000175818"], "unii": ["4AF302ESOS"], "rxcui": ["104894"], "spl_set_id": ["af836a30-5e51-5c97-e053-2995a90a15b9"], "pharm_class_epc": ["Serotonin-3 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Serotonin 3 Receptor Antagonists [MoA]"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (80425-0073-1)", "package_ndc": "80425-0073-1", "marketing_start_date": "20100412"}, {"sample": false, "description": "30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (80425-0073-2)", "package_ndc": "80425-0073-2", "marketing_start_date": "20100412"}], "brand_name": "Ondansetron ODT", "product_id": "80425-0073_2a98d9c1-b777-40b1-e063-6294a90a20e4", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "80425-0073", "generic_name": "Ondansetron", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "brand_name_suffix": "ODT", "active_ingredients": [{"name": "ONDANSETRON", "strength": "4 mg/1"}], "application_number": "ANDA090469", "marketing_category": "ANDA", "marketing_start_date": "20100412", "listing_expiration_date": "20261231"}