Package 0603-4593-15

Brand: methylprednisolone

Generic: methylprednisolone
NDC Package

Package Facts

Identity

Package NDC 0603-4593-15
Digits Only 0603459315
Product NDC 0603-4593
Description

1 DOSE PACK in 1 CARTON (0603-4593-15) / 21 TABLET in 1 DOSE PACK

Marketing

Marketing Status
Marketed Since 1998-12-22
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": "6b210f06-32c0-450a-ad2b-2d0827b06f7a", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0306034593212"], "unii": ["X4W7ZR7023"], "rxcui": ["259966", "762675"], "spl_set_id": ["c84cf5e6-746d-41fb-b3d8-2c0b8ba989af"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 DOSE PACK in 1 CARTON (0603-4593-15)  / 21 TABLET in 1 DOSE PACK", "package_ndc": "0603-4593-15", "marketing_start_date": "19981222"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0603-4593-21)", "package_ndc": "0603-4593-21", "marketing_start_date": "19981222"}], "brand_name": "MethylPREDNISolone", "product_id": "0603-4593_6b210f06-32c0-450a-ad2b-2d0827b06f7a", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0603-4593", "generic_name": "methylprednisolone", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MethylPREDNISolone", "active_ingredients": [{"name": "METHYLPREDNISOLONE", "strength": "4 mg/1"}], "application_number": "ANDA040183", "marketing_category": "ANDA", "marketing_start_date": "19981222", "listing_expiration_date": "20261231"}