Package 42023-238-01

Brand: methylprednisolone acetate

Generic: methylprednisolone acetate
NDC Package

Package Facts

Identity

Package NDC 42023-238-01
Digits Only 4202323801
Product NDC 42023-238
Description

1 VIAL in 1 CARTON (42023-238-01) / 5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2023-11-02
Brand methylprednisolone acetate
Generic methylprednisolone acetate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRA-ARTICULAR", "INTRALESIONAL", "INTRAMENINGEAL", "SOFT TISSUE"], "spl_id": "9d6bd79b-4885-454e-b127-c5978e501024", "openfda": {"unii": ["43502P7F0P"], "rxcui": ["1358610", "1358617"], "spl_set_id": ["631f7d3e-5620-4be3-b918-2f0d38a97890"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (42023-238-01)  / 5 mL in 1 VIAL", "package_ndc": "42023-238-01", "marketing_start_date": "20231102"}], "brand_name": "METHYLPREDNISOLONE ACETATE", "product_id": "42023-238_9d6bd79b-4885-454e-b127-c5978e501024", "dosage_form": "INJECTION, SUSPENSION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "42023-238", "generic_name": "METHYLPREDNISOLONE ACETATE", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHYLPREDNISOLONE ACETATE", "active_ingredients": [{"name": "METHYLPREDNISOLONE ACETATE", "strength": "40 mg/mL"}], "application_number": "ANDA214297", "marketing_category": "ANDA", "marketing_start_date": "20231102", "listing_expiration_date": "20261231"}