ondansetron

Generic: ondansetron

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ondansetron
Generic Name ondansetron
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

ondansetron hydrochloride 2 mg/mL

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-547
Product ID 23155-547_a9ae0d2e-667a-4c29-8697-32b044725d35
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079224
Listing Expiration 2027-12-31
Marketing Start 2012-06-15

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 23155547
Hyphenated Format 23155-547

Supplemental Identifiers

RxCUI
283504 1740467
UNII
NMH84OZK2B

Packaging Origin

Original Packager
true

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 ANDA079224 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2 mg/mL
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (23155-547-41) / 2 mL in 1 VIAL (23155-547-31)
  • 25 VIAL in 1 CARTON (23155-547-42) / 2 mL in 1 VIAL (23155-547-31)
source: ndc

Packages (2)

23155-547-41 10 VIAL in 1 CARTON (23155-547-41) / 2 mL in 1 VIAL (23155-547-31) 23155-547-42 25 VIAL in 1 CARTON (23155-547-42) / 2 mL in 1 VIAL (23155-547-31)

Ingredients (1)

ondansetron hydrochloride (2 mg/mL)

Linked Drug Pages (1)

ONDANSETRON ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "a9ae0d2e-667a-4c29-8697-32b044725d35", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["283504", "1740467"], "spl_set_id": ["b746d4db-43e6-4219-9e6b-f53e59581305"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (23155-547-41)  / 2 mL in 1 VIAL (23155-547-31)", "package_ndc": "23155-547-41", "marketing_start_date": "20120615"}, {"sample": false, "description": "25 VIAL in 1 CARTON (23155-547-42)  / 2 mL in 1 VIAL (23155-547-31)", "package_ndc": "23155-547-42", "marketing_start_date": "20120615"}], "brand_name": "ONDANSETRON", "product_id": "23155-547_a9ae0d2e-667a-4c29-8697-32b044725d35", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "23155-547", "generic_name": "ONDANSETRON", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ONDANSETRON", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA079224", "marketing_category": "ANDA", "marketing_start_date": "20120615", "listing_expiration_date": "20271231"}