Package 72189-254-10

Brand: dexamethasone

Generic: dexamethasone
NDC Package

Package Facts

Identity

Package NDC 72189-254-10
Digits Only 7218925410
Product NDC 72189-254
Description

10 TABLET in 1 BOTTLE (72189-254-10)

Marketing

Marketing Status
Marketed Since 2021-09-20
Brand dexamethasone
Generic dexamethasone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c28e5cd-de70-cb2d-e063-6394a90ab7f2", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["7S5I7G3JQL"], "rxcui": ["197582"], "spl_set_id": ["cc7140de-a205-f675-e053-2995a90ac22b"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Direct Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BOTTLE (72189-254-10)", "package_ndc": "72189-254-10", "marketing_start_date": "20210920"}], "brand_name": "DEXAMETHASONE", "product_id": "72189-254_2c28e5cd-de70-cb2d-e063-6394a90ab7f2", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72189-254", "generic_name": "DEXAMETHASONE", "labeler_name": "Direct Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXAMETHASONE", "active_ingredients": [{"name": "DEXAMETHASONE", "strength": "4 mg/1"}], "application_number": "ANDA084612", "marketing_category": "ANDA", "marketing_start_date": "20210920", "listing_expiration_date": "20261231"}