Package 69306-400-21

Brand: methylprednisolone

Generic: methylprednisolone
NDC Package

Package Facts

Identity

Package NDC 69306-400-21
Digits Only 6930640021
Product NDC 69306-400
Description

21 TABLET in 1 BLISTER PACK (69306-400-21)

Marketing

Marketing Status
Marketed Since 2021-03-18
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": "c479dc26-1a87-14c5-e053-2995a90a8aad", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0369306400212"], "unii": ["X4W7ZR7023"], "rxcui": ["259966"], "spl_set_id": ["c6ec50b5-aeb8-40c3-83e2-af4fe8fefb14"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Doc Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BLISTER PACK (69306-400-21)", "package_ndc": "69306-400-21", "marketing_start_date": "20210318"}], "brand_name": "METHYLPREDNISOLONE", "product_id": "69306-400_c479dc26-1a87-14c5-e053-2995a90a8aad", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "69306-400", "generic_name": "METHYLPREDNISOLONE", "labeler_name": "Doc Rx", "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"}