ondansetron
Generic: ondansetron
Labeler: nucare pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
ondansetron
Generic Name
ondansetron
Labeler
nucare pharmaceuticals, inc.
Dosage Form
TABLET, ORALLY DISINTEGRATING
Routes
Active Ingredients
ondansetron 4 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-3268
Product ID
68071-3268_4c3bfaa1-85d5-5e53-e063-6294a90a84fd
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078152
Listing Expiration
2027-12-31
Marketing Start
2007-06-27
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680713268
Hyphenated Format
68071-3268
Supplemental Identifiers
RxCUI
UPC
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
ANDA078152 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/1
Packaging
- 10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-1)
- 2 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-2)
- 3 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-3)
- 4 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-4)
- 5 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-5)
- 6 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-6)
- 20 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-7)
Packages (7)
68071-3268-1
10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-1)
68071-3268-2
2 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-2)
68071-3268-3
3 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-3)
68071-3268-4
4 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-4)
68071-3268-5
5 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-5)
68071-3268-6
6 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-6)
68071-3268-7
20 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-7)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4c3bfaa1-85d5-5e53-e063-6294a90a84fd", "openfda": {"nui": ["N0000175817", "N0000175818"], "upc": ["0368071326864"], "unii": ["4AF302ESOS"], "rxcui": ["104894"], "spl_set_id": ["50383ef5-6e6e-63a7-e054-00144ff88e88"], "pharm_class_epc": ["Serotonin-3 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Serotonin 3 Receptor Antagonists [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-1)", "package_ndc": "68071-3268-1", "marketing_start_date": "20170523"}, {"sample": false, "description": "2 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-2)", "package_ndc": "68071-3268-2", "marketing_start_date": "20170523"}, {"sample": false, "description": "3 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-3)", "package_ndc": "68071-3268-3", "marketing_start_date": "20170523"}, {"sample": false, "description": "4 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-4)", "package_ndc": "68071-3268-4", "marketing_start_date": "20170523"}, {"sample": false, "description": "5 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-5)", "package_ndc": "68071-3268-5", "marketing_start_date": "20170523"}, {"sample": false, "description": "6 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-6)", "package_ndc": "68071-3268-6", "marketing_start_date": "20170523"}, {"sample": false, "description": "20 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68071-3268-7)", "package_ndc": "68071-3268-7", "marketing_start_date": "20170523"}], "brand_name": "Ondansetron", "product_id": "68071-3268_4c3bfaa1-85d5-5e53-e063-6294a90a84fd", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "68071-3268", "generic_name": "Ondansetron", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON", "strength": "4 mg/1"}], "application_number": "ANDA078152", "marketing_category": "ANDA", "marketing_start_date": "20070627", "listing_expiration_date": "20271231"}