Package 76420-193-21

Brand: methylprednisolone

Generic: methylprednisolone
NDC Package

Package Facts

Identity

Package NDC 76420-193-21
Digits Only 7642019321
Product NDC 76420-193
Description

21 TABLET in 1 BLISTER PACK (76420-193-21)

Marketing

Marketing Status
Marketed Since 2021-03-16
Brand methylprednisolone
Generic methylprednisolone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bda4563a-3fa1-a76b-e053-2995a90a304c", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["X4W7ZR7023"], "rxcui": ["259966", "762675"], "spl_set_id": ["8bff5330-c1f6-4014-aadb-45c1726248dd"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BLISTER PACK (76420-193-21)", "package_ndc": "76420-193-21", "marketing_start_date": "20210316"}], "brand_name": "METHYLPREDNISOLONE", "product_id": "76420-193_bda4563a-3fa1-a76b-e053-2995a90a304c", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "76420-193", "generic_name": "METHYLPREDNISOLONE", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHYLPREDNISOLONE", "active_ingredients": [{"name": "METHYLPREDNISOLONE", "strength": "4 mg/1"}], "application_number": "ANDA204072", "marketing_category": "ANDA", "marketing_start_date": "20180514", "listing_expiration_date": "20261231"}