Package 50268-622-15

Brand: ondansetron hydrochloride

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50268-622-15
Digits Only 5026862215
Product NDC 50268-622
Description

50 BLISTER PACK in 1 BOX (50268-622-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-622-11)

Marketing

Marketing Status
Marketed Since 2016-08-05
Brand ondansetron hydrochloride
Generic ondansetron hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b4a96a8-a177-432e-e063-6294a90a8d5e", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["198052", "312086"], "spl_set_id": ["e4766235-ac44-ca93-78a6-66d4ded33ada"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-622-15)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-622-11)", "package_ndc": "50268-622-15", "marketing_start_date": "20160805"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "50268-622_2b4a96a8-a177-432e-e063-6294a90a8d5e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "50268-622", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron Hydrochloride", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "8 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20160805", "listing_expiration_date": "20261231"}