Package 72189-383-30

Brand: dexamethasone

Generic: dexamethasone
NDC Package

Package Facts

Identity

Package NDC 72189-383-30
Digits Only 7218938330
Product NDC 72189-383
Description

30 TABLET in 1 BOTTLE (72189-383-30)

Marketing

Marketing Status
Marketed Since 2022-09-19
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": "2c4cd6df-c358-b1f7-e063-6394a90a9507", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["7S5I7G3JQL"], "rxcui": ["343033"], "spl_set_id": ["e90cb7f5-5e99-fbf3-e053-2995a90a70aa"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-383-30)", "package_ndc": "72189-383-30", "marketing_start_date": "20220919"}], "brand_name": "Dexamethasone", "product_id": "72189-383_2c4cd6df-c358-b1f7-e063-6394a90a9507", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72189-383", "generic_name": "Dexamethasone", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone", "active_ingredients": [{"name": "DEXAMETHASONE", "strength": ".75 mg/1"}], "application_number": "ANDA084613", "marketing_category": "ANDA", "marketing_start_date": "20220919", "listing_expiration_date": "20261231"}