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
71335-2974
Product ID
71335-2974_104ff98e-4e4c-4e0c-bacd-baee557673da
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209389
Listing Expiration
2026-12-31
Marketing Start
2025-06-19
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
713352974
Hyphenated Format
71335-2974
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
ANDA209389 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 8 mg/1
Packaging
- 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-1)
- 10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-2)
- 9 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-3)
- 5 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-4)
- 3 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-5)
- 6 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-6)
- 12 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-7)
Packages (7)
71335-2974-1
30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-1)
71335-2974-2
10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-2)
71335-2974-3
9 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-3)
71335-2974-4
5 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-4)
71335-2974-5
3 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-5)
71335-2974-6
6 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-6)
71335-2974-7
12 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-7)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "104ff98e-4e4c-4e0c-bacd-baee557673da", "openfda": {"nui": ["N0000175817", "N0000175818"], "unii": ["4AF302ESOS"], "rxcui": ["312087"], "spl_set_id": ["40258e4b-5e67-46c0-8ef0-3e8bfe36ba11"], "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": "30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-1)", "package_ndc": "71335-2974-1", "marketing_start_date": "20251106"}, {"sample": false, "description": "10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-2)", "package_ndc": "71335-2974-2", "marketing_start_date": "20251106"}, {"sample": false, "description": "9 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-3)", "package_ndc": "71335-2974-3", "marketing_start_date": "20251106"}, {"sample": false, "description": "5 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-4)", "package_ndc": "71335-2974-4", "marketing_start_date": "20251106"}, {"sample": false, "description": "3 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-5)", "package_ndc": "71335-2974-5", "marketing_start_date": "20251106"}, {"sample": false, "description": "6 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-6)", "package_ndc": "71335-2974-6", "marketing_start_date": "20251106"}, {"sample": false, "description": "12 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-2974-7)", "package_ndc": "71335-2974-7", "marketing_start_date": "20251106"}], "brand_name": "Ondansetron", "product_id": "71335-2974_104ff98e-4e4c-4e0c-bacd-baee557673da", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "71335-2974", "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": "ANDA209389", "marketing_category": "ANDA", "marketing_start_date": "20250619", "listing_expiration_date": "20261231"}