Package 63323-374-20
Brand: ondansetron
Generic: ondansetron hydrochloridePackage Facts
Identity
Package NDC
63323-374-20
Digits Only
6332337420
Product NDC
63323-374
Description
1 VIAL in 1 BOX (63323-374-20) / 20 mL in 1 VIAL
Marketing
Marketing Status
Brand
ondansetron
Generic
ondansetron hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "83824969-e116-40d6-8940-ff134a4f16c0", "openfda": {"upc": ["0363323374204", "0363323373009"], "unii": ["NMH84OZK2B"], "rxcui": ["283504", "1740467"], "spl_set_id": ["e0050959-c14c-41b6-9a92-fadc5f6feff3"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (63323-374-20) / 20 mL in 1 VIAL", "package_ndc": "63323-374-20", "marketing_start_date": "20091118"}], "brand_name": "Ondansetron", "product_id": "63323-374_83824969-e116-40d6-8940-ff134a4f16c0", "dosage_form": "INJECTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "63323-374", "generic_name": "ONDANSETRON HYDROCHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA076974", "marketing_category": "ANDA", "marketing_start_date": "20091118", "listing_expiration_date": "20261231"}