ondansetron
Generic: ondansetron
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
ondansetron
Generic Name
ondansetron
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET, ORALLY DISINTEGRATING
Routes
Active Ingredients
ondansetron 4 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43063-857
Product ID
43063-857_3ed995a4-00a5-c1d0-e063-6394a90a0298
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
43063857
Hyphenated Format
43063-857
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
ANDA090469 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/1
Packaging
- 2 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-02)
- 4 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-04)
- 5 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-05)
- 6 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-06)
- 8 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-08)
- 10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-10)
- 20 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-20)
Packages (7)
43063-857-02
2 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-02)
43063-857-04
4 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-04)
43063-857-05
5 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-05)
43063-857-06
6 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-06)
43063-857-08
8 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-08)
43063-857-10
10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-10)
43063-857-20
20 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-20)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ed995a4-00a5-c1d0-e063-6394a90a0298", "openfda": {"nui": ["N0000175817", "N0000175818"], "upc": ["0343063857052"], "unii": ["4AF302ESOS"], "rxcui": ["104894"], "spl_set_id": ["9558d296-8edd-4aa1-875a-6247f9a8374d"], "pharm_class_epc": ["Serotonin-3 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Serotonin 3 Receptor Antagonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-02)", "package_ndc": "43063-857-02", "marketing_start_date": "20180604"}, {"sample": false, "description": "4 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-04)", "package_ndc": "43063-857-04", "marketing_start_date": "20180612"}, {"sample": false, "description": "5 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-05)", "package_ndc": "43063-857-05", "marketing_start_date": "20180612"}, {"sample": false, "description": "6 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-06)", "package_ndc": "43063-857-06", "marketing_start_date": "20180604"}, {"sample": false, "description": "8 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-08)", "package_ndc": "43063-857-08", "marketing_start_date": "20180607"}, {"sample": false, "description": "10 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-10)", "package_ndc": "43063-857-10", "marketing_start_date": "20180618"}, {"sample": false, "description": "20 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (43063-857-20)", "package_ndc": "43063-857-20", "marketing_start_date": "20180821"}], "brand_name": "Ondansetron", "product_id": "43063-857_3ed995a4-00a5-c1d0-e063-6394a90a0298", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "43063-857", "generic_name": "Ondansetron", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON", "strength": "4 mg/1"}], "application_number": "ANDA090469", "marketing_category": "ANDA", "marketing_start_date": "20100412", "listing_expiration_date": "20261231"}