methylprednisolone sodium succinate (70121-1000)

Drug Facts

Product Profile

Brand Name methylprednisolone sodium succinate

Generic Name methylprednisolone

Labeler amneal pharmaceuticals llc

Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Routes

INTRAMUSCULAR INTRAVENOUS

Active Ingredients

methylprednisolone sodium succinate 40 mg/mL

Manufacturer

Amneal Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 70121-1000

Product ID 70121-1000_3eb27de6-9e1c-4ef4-bb31-2458b9360582

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA207549

Listing Expiration 2026-12-31

Marketing Start 2016-11-11

Pharmacologic Class

Classes

corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 701211000

Hyphenated Format 70121-1000

Supplemental Identifiers

RxCUI

311659 1743704

UPC

0370121100010 0370121100119

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 ANDA207549 (source: ndc)

Routes

INTRAMUSCULAR INTRAVENOUS

source: ndc

Resolved Composition

Strengths

40 mg/mL

source: ndc

Packaging

25 VIAL in 1 CARTON (70121-1000-5) / 1 mL in 1 VIAL (70121-1000-1)

source: ndc

Packages (1)

70121-1000-5 25 VIAL in 1 CARTON (70121-1000-5) / 1 mL in 1 VIAL (70121-1000-1)

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": "3eb27de6-9e1c-4ef4-bb31-2458b9360582", "openfda": {"upc": ["0370121100010", "0370121100119"], "unii": ["LEC9GKY20K"], "rxcui": ["311659", "1743704"], "spl_set_id": ["e86fbda8-00e4-4d54-841a-59dea6c15e70"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70121-1000-5)  / 1 mL in 1 VIAL (70121-1000-1)", "package_ndc": "70121-1000-5", "marketing_start_date": "20161111"}], "brand_name": "Methylprednisolone Sodium Succinate", "product_id": "70121-1000_3eb27de6-9e1c-4ef4-bb31-2458b9360582", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70121-1000", "generic_name": "Methylprednisolone", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylprednisolone Sodium Succinate", "active_ingredients": [{"name": "METHYLPREDNISOLONE SODIUM SUCCINATE", "strength": "40 mg/mL"}], "application_number": "ANDA207549", "marketing_category": "ANDA", "marketing_start_date": "20161111", "listing_expiration_date": "20261231"}