Package 68084-220-01

Brand: ondansetron hydrochloride

Generic: ondansetron hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68084-220-01
Digits Only 6808422001
Product NDC 68084-220
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-220-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-220-11)

Marketing

Marketing Status
Marketed Since 2023-09-21
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": "276fcece-7658-5e70-e063-6394a90a91ae", "openfda": {"unii": ["NMH84OZK2B"], "rxcui": ["198052", "312086"], "spl_set_id": ["9f015e60-1aec-4ae7-b28f-42f6c8f50455"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-220-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-220-11)", "package_ndc": "68084-220-01", "marketing_start_date": "20230921"}], "brand_name": "Ondansetron Hydrochloride", "product_id": "68084-220_276fcece-7658-5e70-e063-6394a90a91ae", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin 3 Receptor Antagonists [MoA]", "Serotonin-3 Receptor Antagonist [EPC]"], "product_ndc": "68084-220", "generic_name": "Ondansetron Hydrochloride", "labeler_name": "American Health Packaging", "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": "20230921", "listing_expiration_date": "20261231"}