Package 72789-501-20
Brand: dexamethasone
Generic: dexamethasonePackage Facts
Identity
Package NDC
72789-501-20
Digits Only
7278950120
Product NDC
72789-501
Description
20 TABLET in 1 BOTTLE, PLASTIC (72789-501-20)
Marketing
Marketing Status
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": "3402e8cb-d2c8-1bbf-e063-6294a90abb34", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0372789501208"], "unii": ["7S5I7G3JQL"], "rxcui": ["343033"], "spl_set_id": ["a5609df4-4933-4f85-a7b8-bc54a70a2bac"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (72789-501-20)", "package_ndc": "72789-501-20", "marketing_start_date": "20250430"}], "brand_name": "Dexamethasone", "product_id": "72789-501_3402e8cb-d2c8-1bbf-e063-6294a90abb34", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72789-501", "generic_name": "Dexamethasone", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone", "active_ingredients": [{"name": "DEXAMETHASONE", "strength": ".75 mg/1"}], "application_number": "ANDA216282", "marketing_category": "ANDA", "marketing_start_date": "20240415", "listing_expiration_date": "20261231"}