Package 70518-4320-0

Brand: dexamethasone

Generic: dexamethasone
NDC Package

Package Facts

Identity

Package NDC 70518-4320-0
Digits Only 7051843200
Product NDC 70518-4320
Description

4 TABLET in 1 BOTTLE, PLASTIC (70518-4320-0)

Marketing

Marketing Status
Marketed Since 2025-03-25
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": "402e606f-d63d-9455-e063-6394a90a5994", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["7S5I7G3JQL"], "rxcui": ["197582"], "spl_set_id": ["8c5375a7-7a0d-4af0-8b86-bc87698ac3d1"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BOTTLE, PLASTIC (70518-4320-0)", "package_ndc": "70518-4320-0", "marketing_start_date": "20250325"}], "brand_name": "Dexamethasone", "product_id": "70518-4320_402e606f-d63d-9455-e063-6394a90a5994", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70518-4320", "generic_name": "Dexamethasone", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone", "active_ingredients": [{"name": "DEXAMETHASONE", "strength": "4 mg/1"}], "application_number": "ANDA215604", "marketing_category": "ANDA", "marketing_start_date": "20250325", "listing_expiration_date": "20261231"}