methylprednisolone

Generic: methylprednisolone

Labeler: preferred pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methylprednisolone
Generic Name methylprednisolone
Labeler preferred pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methylprednisolone 4 mg/1

Manufacturer
Preferred Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68788-4593
Product ID 68788-4593_da53e590-2763-49f9-a735-9a1794b8aec4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040189
Marketing Start 2013-09-03
Marketing End 2026-04-30

Pharmacologic Class

Established (EPC)
corticosteroid [epc]
Mechanism of Action
corticosteroid hormone receptor agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687884593
Hyphenated Format 68788-4593

Supplemental Identifiers

RxCUI
259966 762675
UNII
X4W7ZR7023
NUI
N0000175576 N0000175450

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 (source: ndc)
Generic Name methylprednisolone (source: ndc)
Application Number ANDA040189 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 21 TABLET in 1 BLISTER PACK (68788-4593-2)
source: ndc

Packages (1)

68788-4593-2 21 TABLET in 1 BLISTER PACK (68788-4593-2)

Ingredients (1)

methylprednisolone (4 mg/1)

Linked Drug Pages (1)

Methylprednisolone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "da53e590-2763-49f9-a735-9a1794b8aec4", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["X4W7ZR7023"], "rxcui": ["259966", "762675"], "spl_set_id": ["ebe4f4a5-3fec-4f30-8289-25e594162c49"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BLISTER PACK (68788-4593-2)", "package_ndc": "68788-4593-2", "marketing_end_date": "20260430", "marketing_start_date": "20130903"}], "brand_name": "Methylprednisolone", "product_id": "68788-4593_da53e590-2763-49f9-a735-9a1794b8aec4", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68788-4593", "generic_name": "Methylprednisolone", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylprednisolone", "active_ingredients": [{"name": "METHYLPREDNISOLONE", "strength": "4 mg/1"}], "application_number": "ANDA040189", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20130903"}