Package 51655-933-43

Brand: ondansetron hydrochloride

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-933-43
Digits Only 5165593343
Product NDC 51655-933
Description

3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-43)

Marketing

Marketing Status
Marketed Since 2022-07-20
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": "4960f7bf-1a44-0802-e063-6394a90a2855", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["198052"], "spl_set_id": ["f76d27c5-acd4-482c-e053-6294a90a5284"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-04)", "package_ndc": "51655-933-04", "marketing_start_date": "20221025"}, {"sample": false, "description": "3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-43)", "package_ndc": "51655-933-43", "marketing_start_date": "20220720"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-53)", "package_ndc": "51655-933-53", "marketing_start_date": "20220916"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-54)", "package_ndc": "51655-933-54", "marketing_start_date": "20230511"}, {"sample": false, "description": "5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-55)", "package_ndc": "51655-933-55", "marketing_start_date": "20230509"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-933-87)", "package_ndc": "51655-933-87", "marketing_start_date": "20220720"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "51655-933_4960f7bf-1a44-0802-e063-6394a90a2855", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "51655-933", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ondansetron Hydrochloride", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20220720", "listing_expiration_date": "20271231"}