ondansetron

Generic: ondansetron

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ondansetron
Generic Name ondansetron
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET, ORALLY DISINTEGRATING
Routes
ORAL
Active Ingredients

ondansetron 4 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 62756-240
Product ID 62756-240_e83d90db-54a7-4c13-bd68-b1620a8aecaf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077557
Listing Expiration 2026-12-31
Marketing Start 2007-08-02

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 62756240
Hyphenated Format 62756-240

Supplemental Identifiers

RxCUI
104894 198052 312086 312087
UPC
0362756131019 0362756240834 0362756240643 0362756356832 0362756130012
UNII
4AF302ESOS NMH84OZK2B
NUI
N0000175817 N0000175818

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 ondansetron (source: ndc)
Generic Name ondansetron (source: ndc)
Application Number ANDA077557 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 3 BLISTER PACK in 1 DOSE PACK (62756-240-64) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
  • 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (62756-240-83)
source: ndc

Packages (2)

62756-240-64 3 BLISTER PACK in 1 DOSE PACK (62756-240-64) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK 62756-240-83 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (62756-240-83)

Ingredients (1)

ondansetron (4 mg/1)

Linked Drug Pages (1)

ondansetron hydrochloride, ondansetron ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e83d90db-54a7-4c13-bd68-b1620a8aecaf", "openfda": {"nui": ["N0000175817", "N0000175818"], "upc": ["0362756131019", "0362756240834", "0362756240643", "0362756356832", "0362756130012"], "unii": ["4AF302ESOS", "NMH84OZK2B"], "rxcui": ["104894", "198052", "312086", "312087"], "spl_set_id": ["92c758a3-e749-4a15-be4b-ee30b364b2b0"], "pharm_class_epc": ["Serotonin-3 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Serotonin 3 Receptor Antagonists [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 DOSE PACK (62756-240-64)  / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "62756-240-64", "marketing_start_date": "20070802"}, {"sample": false, "description": "30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (62756-240-83)", "package_ndc": "62756-240-83", "marketing_start_date": "20070802"}], "brand_name": "ondansetron", "product_id": "62756-240_e83d90db-54a7-4c13-bd68-b1620a8aecaf", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "62756-240", "generic_name": "ondansetron", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ondansetron", "active_ingredients": [{"name": "ONDANSETRON", "strength": "4 mg/1"}], "application_number": "ANDA077557", "marketing_category": "ANDA", "marketing_start_date": "20070802", "listing_expiration_date": "20261231"}