Package 68084-220-01
Brand: ondansetron hydrochloride
Generic: ondansetron hydrochloridePackage 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
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"}