Package 43063-792-06

Brand: ondansetron hydrochloride

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-792-06
Digits Only 4306379206
Product NDC 43063-792
Description

6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-792-06)

Marketing

Marketing Status
Marketed Since 2017-10-06
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": "3ed9a18c-3975-d837-e063-6394a90a8f1e", "openfda": {"upc": ["0343063792063"], "unii": ["NMH84OZK2B"], "rxcui": ["312086"], "spl_set_id": ["0b675b09-fe40-435c-b91a-c61cdf767fbf"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-792-06)", "package_ndc": "43063-792-06", "marketing_start_date": "20171006"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "43063-792_3ed9a18c-3975-d837-e063-6394a90a8f1e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "43063-792", "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": "8 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20070731", "listing_expiration_date": "20261231"}