ondansetron
Generic: ondansetron
Labeler: preferred pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
ondansetron
Generic Name
ondansetron
Labeler
preferred pharmaceuticals, inc.
Dosage Form
TABLET, ORALLY DISINTEGRATING
Routes
Active Ingredients
ondansetron 8 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-9559
Product ID
68788-9559_f31d49c2-beda-452d-9f36-f1ef89a0eeae
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090469
Listing Expiration
2026-12-31
Marketing Start
2013-08-27
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687889559
Hyphenated Format
68788-9559
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA090469 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 8 mg/1
Packaging
- 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (68788-9559-1)
- 3 BLISTER PACK in 1 CARTON (68788-9559-3) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
- 5 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68788-9559-5)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f31d49c2-beda-452d-9f36-f1ef89a0eeae", "openfda": {"nui": ["N0000175817", "N0000175818"], "unii": ["4AF302ESOS"], "rxcui": ["312087"], "spl_set_id": ["b9abd5ce-6aca-4fda-8f46-0bb5b7fdd5da"], "pharm_class_epc": ["Serotonin-3 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Serotonin 3 Receptor Antagonists [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (68788-9559-1)", "package_ndc": "68788-9559-1", "marketing_start_date": "20130827"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (68788-9559-3) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "68788-9559-3", "marketing_start_date": "20130827"}, {"sample": false, "description": "5 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68788-9559-5)", "package_ndc": "68788-9559-5", "marketing_start_date": "20130827"}], "brand_name": "Ondansetron", "product_id": "68788-9559_f31d49c2-beda-452d-9f36-f1ef89a0eeae", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "68788-9559", "generic_name": "Ondansetron", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON", "strength": "8 mg/1"}], "application_number": "ANDA090469", "marketing_category": "ANDA", "marketing_start_date": "20130827", "listing_expiration_date": "20261231"}