Package 55111-153-78

Brand: ondansetron

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55111-153-78
Digits Only 5511115378
Product NDC 55111-153
Description

10 DOSE PACK in 1 BOX (55111-153-78) / 10 TABLET, FILM COATED in 1 DOSE PACK

Marketing

Marketing Status
Marketed Since 2006-12-26
Brand ondansetron
Generic ondansetron hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b5be4b6c-42cd-c9b3-a0df-e15c946ec89b", "openfda": {"upc": ["0355111153306", "0355111154303"], "unii": ["NMH84OZK2B"], "rxcui": ["198052", "312084", "312086"], "spl_set_id": ["162f2088-9fb1-47e7-b88c-45104be7e7bb"], "manufacturer_name": ["Dr. Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (55111-153-01)", "package_ndc": "55111-153-01", "marketing_start_date": "20061226"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (55111-153-05)", "package_ndc": "55111-153-05", "marketing_start_date": "20061226"}, {"sample": false, "description": "3 DOSE PACK in 1 BOX (55111-153-13)  / 1 TABLET, FILM COATED in 1 DOSE PACK", "package_ndc": "55111-153-13", "marketing_start_date": "20061226"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (55111-153-30)", "package_ndc": "55111-153-30", "marketing_start_date": "20061226"}, {"sample": false, "description": "10 DOSE PACK in 1 BOX (55111-153-78)  / 10 TABLET, FILM COATED in 1 DOSE PACK", "package_ndc": "55111-153-78", "marketing_start_date": "20061226"}], "brand_name": "ONDANSETRON", "product_id": "55111-153_b5be4b6c-42cd-c9b3-a0df-e15c946ec89b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "55111-153", "generic_name": "ONDANSETRON HYDROCHLORIDE", "labeler_name": "Dr. Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ONDANSETRON", "active_ingredients": [{"name": "ONDANSETRON HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA076183", "marketing_category": "ANDA", "marketing_start_date": "20061226", "listing_expiration_date": "20261231"}