Package 36000-012-25
Brand: ondansetron hydrochloride
Generic: ondansetron hydrochloridePackage Facts
Identity
Package NDC
36000-012-25
Digits Only
3600001225
Product NDC
36000-012
Description
25 VIAL, SINGLE-DOSE in 1 CARTON (36000-012-25) / 2 mL in 1 VIAL, SINGLE-DOSE
Marketing
Marketing Status
Brand
ondansetron hydrochloride
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": "f917f6a4-bb84-46ed-ba13-68e4c01097e6", "openfda": {"upc": ["0336000012256"], "unii": ["NMH84OZK2B"], "rxcui": ["283504", "1740467"], "spl_set_id": ["729d865f-d84a-495e-9456-4bceebb6e03f"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (36000-012-25) / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "36000-012-25", "marketing_start_date": "20130313"}], "brand_name": "ONDANSETRON HYDROCHLORIDE", "product_id": "36000-012_f917f6a4-bb84-46ed-ba13-68e4c01097e6", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "36000-012", "generic_name": "ONDANSETRON HYDROCHLORIDE", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ONDANSETRON HYDROCHLORIDE", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "2 mg/mL"}], "application_number": "ANDA078287", "marketing_category": "ANDA", "marketing_start_date": "20130313", "listing_expiration_date": "20261231"}