methylprednisolone sodium succinate

Generic: methylprednisolone sodium succinate

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methylprednisolone sodium succinate
Generic Name methylprednisolone sodium succinate
Labeler hikma pharmaceuticals usa inc.
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

methylprednisolone sodium succinate 1 g/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9851
Product ID 0143-9851_833d62b5-a589-4ea8-ad41-82d08d2d4589
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202691
Listing Expiration 2026-12-31
Marketing Start 2016-01-01

Pharmacologic Class

Classes
corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439851
Hyphenated Format 0143-9851

Supplemental Identifiers

RxCUI
314099
UNII
LEC9GKY20K

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name methylprednisolone sodium succinate (source: ndc)
Generic Name methylprednisolone sodium succinate (source: ndc)
Application Number ANDA202691 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, MULTI-DOSE (0143-9851-01)
source: ndc

Packages (1)

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

Ingredients (1)

methylprednisolone sodium succinate (1 g/1)

Linked Drug Pages (1)

Methylprednisolone Sodium Succinate ndc-match (0.9)

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"}