ondansetron
Generic: ondansetron
Labeler: bryant ranch prepackDrug Facts
Product Profile
Brand Name
ondansetron
Generic Name
ondansetron
Labeler
bryant ranch prepack
Dosage Form
TABLET, ORALLY DISINTEGRATING
Routes
Active Ingredients
ondansetron 8 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71335-1731
Product ID
71335-1731_bc491a5a-1f19-4c2b-85f3-459d571603a8
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)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713351731
Hyphenated Format
71335-1731
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
- 3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-0)
- 30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-1)
- 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-2)
- 5 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-3)
- 4 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-4)
- 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-5)
- 14 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-6)
- 60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-7)
- 12 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-8)
- 90 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-9)
Packages (10)
71335-1731-0
3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-0)
71335-1731-1
30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-1)
71335-1731-2
10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-2)
71335-1731-3
5 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-3)
71335-1731-4
4 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-4)
71335-1731-5
6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-5)
71335-1731-6
14 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-6)
71335-1731-7
60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-7)
71335-1731-8
12 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-8)
71335-1731-9
90 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-9)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bc491a5a-1f19-4c2b-85f3-459d571603a8", "openfda": {"nui": ["N0000175817", "N0000175818"], "unii": ["4AF302ESOS"], "rxcui": ["312087"], "spl_set_id": ["2d1b8953-7ff5-4e91-ba97-3ba5c6ea8f71"], "pharm_class_epc": ["Serotonin-3 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Serotonin 3 Receptor Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-0)", "package_ndc": "71335-1731-0", "marketing_start_date": "20240404"}, {"sample": false, "description": "30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-1)", "package_ndc": "71335-1731-1", "marketing_start_date": "20210128"}, {"sample": false, "description": "10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-2)", "package_ndc": "71335-1731-2", "marketing_start_date": "20210105"}, {"sample": false, "description": "5 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-3)", "package_ndc": "71335-1731-3", "marketing_start_date": "20201229"}, {"sample": false, "description": "4 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-4)", "package_ndc": "71335-1731-4", "marketing_start_date": "20210524"}, {"sample": false, "description": "6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-5)", "package_ndc": "71335-1731-5", "marketing_start_date": "20201228"}, {"sample": false, "description": "14 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-6)", "package_ndc": "71335-1731-6", "marketing_start_date": "20240404"}, {"sample": false, "description": "60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-7)", "package_ndc": "71335-1731-7", "marketing_start_date": "20240404"}, {"sample": false, "description": "12 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-8)", "package_ndc": "71335-1731-8", "marketing_start_date": "20240404"}, {"sample": false, "description": "90 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (71335-1731-9)", "package_ndc": "71335-1731-9", "marketing_start_date": "20240404"}], "brand_name": "Ondansetron", "product_id": "71335-1731_bc491a5a-1f19-4c2b-85f3-459d571603a8", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "71335-1731", "generic_name": "Ondansetron", "labeler_name": "Bryant Ranch Prepack", "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": "20100412", "listing_expiration_date": "20261231"}