methylprednisolone sodium succinate

Generic: methylprednisolone

Labeler: tianjin kingyork pharmaceuticals co., ltd
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methylprednisolone sodium succinate
Generic Name methylprednisolone
Labeler tianjin kingyork pharmaceuticals co., ltd
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

methylprednisolone sodium succinate 40 mg/mL

Manufacturer
Tianjin Kingyork Pharmaceuticals Co., Ltd

Identifiers & Regulatory

Product NDC 82094-401
Product ID 82094-401_94c8ce6b-7622-4d1f-8b54-0ce959752ae5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212396
Listing Expiration 2026-12-31
Marketing Start 2021-04-20

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82094401
Hyphenated Format 82094-401

Supplemental Identifiers

RxCUI
311659 314099 1357886 1743704
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 (source: ndc)
Application Number ANDA212396 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 40 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (82094-401-50) / 1 mL in 1 VIAL (82094-401-01)
source: ndc

Packages (1)

82094-401-50 25 VIAL in 1 CARTON (82094-401-50) / 1 mL in 1 VIAL (82094-401-01)

Ingredients (1)

methylprednisolone sodium succinate (40 mg/mL)

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": "94c8ce6b-7622-4d1f-8b54-0ce959752ae5", "openfda": {"unii": ["LEC9GKY20K"], "rxcui": ["311659", "314099", "1357886", "1743704"], "spl_set_id": ["77a8d96c-37df-4f3a-9757-b2d4131ff82b"], "manufacturer_name": ["Tianjin Kingyork Pharmaceuticals Co., Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (82094-401-50)  / 1 mL in 1 VIAL (82094-401-01)", "package_ndc": "82094-401-50", "marketing_start_date": "20210420"}], "brand_name": "Methylprednisolone Sodium Succinate", "product_id": "82094-401_94c8ce6b-7622-4d1f-8b54-0ce959752ae5", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "82094-401", "generic_name": "Methylprednisolone", "labeler_name": "Tianjin Kingyork Pharmaceuticals Co., Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylprednisolone Sodium Succinate", "active_ingredients": [{"name": "METHYLPREDNISOLONE SODIUM SUCCINATE", "strength": "40 mg/mL"}], "application_number": "ANDA212396", "marketing_category": "ANDA", "marketing_start_date": "20210420", "listing_expiration_date": "20261231"}