Package 0143-9851-01

Brand: methylprednisolone sodium succinate

Generic: methylprednisolone sodium succinate
NDC Package

Package Facts

Identity

Package NDC 0143-9851-01
Digits Only 0143985101
Product NDC 0143-9851
Product ID 0143-9851_833d62b5-a589-4ea8-ad41-82d08d2d4589
Description

1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, MULTI-DOSE (0143-9851-01)

Marketing

Marketing Status
Marketed Since 2016-01-01
Brand methylprednisolone sodium succinate
Generic methylprednisolone sodium succinate
Sample Package No

Linked Drug Pages (1)

Methylprednisolone Sodium Succinate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "833d62b5-a589-4ea8-ad41-82d08d2d4589", "openfda": {"unii": ["LEC9GKY20K"], "rxcui": ["314099"], "spl_set_id": ["2e540674-0915-4498-8e2b-751c7e97532a"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, MULTI-DOSE (0143-9851-01)", "package_ndc": "0143-9851-01", "marketing_start_date": "20160101"}], "brand_name": "Methylprednisolone Sodium Succinate", "product_id": "0143-9851_833d62b5-a589-4ea8-ad41-82d08d2d4589", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0143-9851", "generic_name": "Methylprednisolone Sodium Succinate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylprednisolone Sodium Succinate", "active_ingredients": [{"name": "METHYLPREDNISOLONE SODIUM SUCCINATE", "strength": "1 g/1"}], "application_number": "ANDA202691", "marketing_category": "ANDA", "marketing_start_date": "20160101", "listing_expiration_date": "20261231"}