solu-medrol(r) methylprednisolone sodium succinat
Generic: solu-medrol(r) methylprednisolone sodium succinat
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
solu-medrol(r) methylprednisolone sodium succinat
Generic Name
solu-medrol(r) methylprednisolone sodium succinat
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
methylprednisolone sodium succinate 500 mg/4mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1483
Product ID
51662-1483_2b39b839-0c7c-de03-e063-6294a90a243e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA011856
Listing Expiration
2026-12-31
Marketing Start
2019-12-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621483
Hyphenated Format
51662-1483
Supplemental Identifiers
RxCUI
UPC
UNII
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
solu-medrol(r) methylprednisolone sodium succinat (source: ndc)
Generic Name
solu-medrol(r) methylprednisolone sodium succinat (source: ndc)
Application Number
NDA011856 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/4mL
Packaging
- 1 VIAL in 1 CARTON (51662-1483-1) / 4 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "2b39b839-0c7c-de03-e063-6294a90a243e", "openfda": {"upc": ["0300090003029"], "unii": ["LEC9GKY20K"], "rxcui": ["1743720"], "spl_set_id": ["99b3c99a-79d5-6c54-e053-2a95a90a28bc"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (51662-1483-1) / 4 mL in 1 VIAL", "package_ndc": "51662-1483-1", "marketing_start_date": "20191214"}], "brand_name": "SOLU-MEDROL(R) METHYLPREDNISOLONE SODIUM SUCCINAT", "product_id": "51662-1483_2b39b839-0c7c-de03-e063-6294a90a243e", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51662-1483", "generic_name": "SOLU-MEDROL(R) METHYLPREDNISOLONE SODIUM SUCCINAT", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SOLU-MEDROL(R) METHYLPREDNISOLONE SODIUM SUCCINAT", "active_ingredients": [{"name": "METHYLPREDNISOLONE SODIUM SUCCINATE", "strength": "500 mg/4mL"}], "application_number": "NDA011856", "marketing_category": "NDA", "marketing_start_date": "20191214", "listing_expiration_date": "20261231"}