Package 43063-770-06

Brand: ondansetron

Generic: ondansetron
NDC Package

Package Facts

Identity

Package NDC 43063-770-06
Digits Only 4306377006
Product NDC 43063-770
Product ID 43063-770_48d46d34-3176-1749-e063-6394a90a9a42
Description

6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-770-06)

Marketing

Marketing Status
Marketed Since 2014-03-03
Brand ondansetron
Generic ondansetron
Sample Package No

Linked Drug Pages (1)

Ondansetron ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "48d46d34-3176-1749-e063-6394a90a9a42", "openfda": {"upc": ["0343063770061"], "unii": ["NMH84OZK2B"], "rxcui": ["312086"], "spl_set_id": ["15d0a711-ef3b-4d93-8fbc-17a45f96af8a"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-770-06)", "package_ndc": "43063-770-06", "marketing_start_date": "20140303"}], "brand_name": "Ondansetron", "product_id": "43063-770_48d46d34-3176-1749-e063-6394a90a9a42", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "43063-770", "generic_name": "Ondansetron", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "8 mg/1"}], "application_number": "ANDA077535", "marketing_category": "ANDA", "marketing_start_date": "20070625", "listing_expiration_date": "20271231"}