ondansetron hydrochloride

Generic: ondansetron hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ondansetron hydrochloride
Generic Name ondansetron hydrochloride
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

ondansetron hydrochloride 4 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-034
Product ID 72789-034_3c6d1f46-ae20-8bc0-e063-6394a90a4a08
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078539
Listing Expiration 2026-12-31
Marketing Start 2007-07-31

Pharmacologic Class

Classes
serotonin 3 receptor antagonists [moa] serotonin-3 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789034
Hyphenated Format 72789-034

Supplemental Identifiers

RxCUI
198052
UPC
0372789034126
UNII
NMH84OZK2B

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 hydrochloride (source: ndc)
Generic Name ondansetron hydrochloride (source: ndc)
Application Number ANDA078539 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-034-12)
source: ndc

Packages (1)

72789-034-12 12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-034-12)

Ingredients (1)

ondansetron hydrochloride (4 mg/1)

Linked Drug Pages (1)

Ondansetron Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3c6d1f46-ae20-8bc0-e063-6394a90a4a08", "openfda": {"upc": ["0372789034126"], "unii": ["NMH84OZK2B"], "rxcui": ["198052"], "spl_set_id": ["426ba54f-199a-41d1-8c27-f827bea56854"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-034-12)", "package_ndc": "72789-034-12", "marketing_start_date": "20191202"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "72789-034_3c6d1f46-ae20-8bc0-e063-6394a90a4a08", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "72789-034", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron Hydrochloride", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20070731", "listing_expiration_date": "20261231"}