Package 69452-276-20

Brand: dexamethasone

Generic: dexamethasone
NDC Package

Package Facts

Identity

Package NDC 69452-276-20
Digits Only 6945227620
Product NDC 69452-276
Description

100 TABLET in 1 BOTTLE (69452-276-20)

Marketing

Marketing Status
Marketed Since 2023-08-01
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": "2f9d9872-68d7-cdc2-e063-6294a90a6463", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["7S5I7G3JQL"], "rxcui": ["197581"], "spl_set_id": ["401ec088-984a-49ab-b317-747c2b9b9e22"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Bionpharma Inc.,"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69452-276-20)", "package_ndc": "69452-276-20", "marketing_start_date": "20230801"}], "brand_name": "Dexamethasone", "product_id": "69452-276_2f9d9872-68d7-cdc2-e063-6294a90a6463", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "69452-276", "generic_name": "Dexamethasone", "labeler_name": "Bionpharma Inc.,", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone", "active_ingredients": [{"name": "DEXAMETHASONE", "strength": "2 mg/1"}], "application_number": "ANDA217538", "marketing_category": "ANDA", "marketing_start_date": "20230801", "listing_expiration_date": "20261231"}