ondansetron

Generic: ondansetron

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ondansetron
Generic Name ondansetron
Labeler redpharm drug
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ondansetron hydrochloride 4 mg/1

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-2119
Product ID 67296-2119_4698a594-cf21-0365-e063-6294a90a8784
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077535
Listing Expiration 2026-12-31
Marketing Start 2007-06-25

Pharmacologic Class

Classes
serotonin 3 receptor antagonists [moa] serotonin-3 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 672962119
Hyphenated Format 67296-2119

Supplemental Identifiers

RxCUI
198052
UPC
0368462158111 0368462106303
UNII
NMH84OZK2B

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 ANDA077535 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (67296-2119-3)
source: ndc

Packages (1)

67296-2119-3 30 TABLET, FILM COATED in 1 BOTTLE (67296-2119-3)

Ingredients (1)

ondansetron hydrochloride (4 mg/1)

Linked Drug Pages (1)

Ondansetron ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4698a594-cf21-0365-e063-6294a90a8784", "openfda": {"upc": ["0368462158111", "0368462106303"], "unii": ["NMH84OZK2B"], "rxcui": ["198052"], "spl_set_id": ["300b1916-a3d8-0220-e063-6394a90a6f55"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (67296-2119-3)", "package_ndc": "67296-2119-3", "marketing_start_date": "20070625"}], "brand_name": "Ondansetron", "product_id": "67296-2119_4698a594-cf21-0365-e063-6294a90a8784", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "67296-2119", "generic_name": "Ondansetron", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA077535", "marketing_category": "ANDA", "marketing_start_date": "20070625", "listing_expiration_date": "20261231"}