Package 61919-565-30

Brand: ondansetron

Generic: ondansetron
NDC Package

Package Facts

Identity

Package NDC 61919-565-30
Digits Only 6191956530
Product NDC 61919-565
Description

30 TABLET, FILM COATED in 1 BOTTLE (61919-565-30)

Marketing

Marketing Status
Marketed Since 2019-08-22
Brand ondansetron
Generic ondansetron
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4b32211f-c9b5-5ea2-e063-6394a90a2834", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["198052"], "spl_set_id": ["90b73778-2ab5-5460-e053-2a95a90abbc1"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (61919-565-30)", "package_ndc": "61919-565-30", "marketing_start_date": "20190822"}, {"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE (61919-565-45)", "package_ndc": "61919-565-45", "marketing_start_date": "20190822"}], "brand_name": "ONDANSETRON", "product_id": "61919-565_4b32211f-c9b5-5ea2-e063-6394a90a2834", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "61919-565", "generic_name": "ONDANSETRON", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ONDANSETRON", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA078539", "marketing_category": "ANDA", "marketing_start_date": "20190822", "listing_expiration_date": "20271231"}