methylprednisolone
Generic: methylprednisolone
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
methylprednisolone
Generic Name
methylprednisolone
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
methylprednisolone 4 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55289-649
Product ID
55289-649_30c9fcb5-73bc-2f23-e063-6294a90a8ab4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040183
Listing Expiration
2026-12-31
Marketing Start
1998-12-22
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55289649
Hyphenated Format
55289-649
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
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
ANDA040183 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (55289-649-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "30c9fcb5-73bc-2f23-e063-6294a90a8ab4", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0355289649304"], "unii": ["X4W7ZR7023"], "rxcui": ["259966"], "spl_set_id": ["a14c4f76-6dd5-4c84-b6e5-e5abf19ab559"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (55289-649-30)", "package_ndc": "55289-649-30", "marketing_start_date": "20160812"}], "brand_name": "MethylPREDNISolone", "product_id": "55289-649_30c9fcb5-73bc-2f23-e063-6294a90a8ab4", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "55289-649", "generic_name": "methylprednisolone", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MethylPREDNISolone", "active_ingredients": [{"name": "METHYLPREDNISOLONE", "strength": "4 mg/1"}], "application_number": "ANDA040183", "marketing_category": "ANDA", "marketing_start_date": "19981222", "listing_expiration_date": "20261231"}