methylprednisolone sodium succinate
Generic: methylprednisolone sodium succinate
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
methylprednisolone sodium succinate
Generic Name
methylprednisolone sodium succinate
Labeler
remedyrepack inc.
Dosage Form
INJECTION
Routes
Active Ingredients
methylprednisolone sodium succinate 125 mg/2mL
Manufacturer
Identifiers & Regulatory
Product NDC
70518-3684
Product ID
70518-3684_3b032f5a-4c8c-b4d7-e063-6294a90aab73
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212396
Listing Expiration
2026-12-31
Marketing Start
2023-03-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705183684
Hyphenated Format
70518-3684
Supplemental Identifiers
RxCUI
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
methylprednisolone sodium succinate (source: ndc)
Generic Name
methylprednisolone sodium succinate (source: ndc)
Application Number
ANDA212396 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 125 mg/2mL
Packaging
- 25 VIAL, SINGLE-DOSE in 1 CARTON (70518-3684-0) / 2 mL in 1 VIAL, SINGLE-DOSE (70518-3684-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "3b032f5a-4c8c-b4d7-e063-6294a90aab73", "openfda": {"unii": ["LEC9GKY20K"], "rxcui": ["1743704"], "spl_set_id": ["f339882f-c380-4022-bdcd-94556a7926aa"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (70518-3684-0) / 2 mL in 1 VIAL, SINGLE-DOSE (70518-3684-1)", "package_ndc": "70518-3684-0", "marketing_start_date": "20230317"}], "brand_name": "Methylprednisolone sodium succinate", "product_id": "70518-3684_3b032f5a-4c8c-b4d7-e063-6294a90aab73", "dosage_form": "INJECTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70518-3684", "generic_name": "Methylprednisolone sodium succinate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylprednisolone sodium succinate", "active_ingredients": [{"name": "METHYLPREDNISOLONE SODIUM SUCCINATE", "strength": "125 mg/2mL"}], "application_number": "ANDA212396", "marketing_category": "ANDA", "marketing_start_date": "20230317", "listing_expiration_date": "20261231"}