methylprednisolone

Generic: methylprednisolone

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methylprednisolone
Generic Name methylprednisolone
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methylprednisolone 4 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3811
Product ID 50090-3811_6bfd8b00-0c6c-40cb-b0dc-677d8d0d0563
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206751
Listing Expiration 2027-12-31
Marketing Start 2018-05-01

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 500903811
Hyphenated Format 50090-3811

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 ANDA206751 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (50090-3811-0) / 21 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

methylprednisolone (4 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6bfd8b00-0c6c-40cb-b0dc-677d8d0d0563", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["X4W7ZR7023"], "rxcui": ["259966", "762675"], "spl_set_id": ["646bb826-8d5a-4b03-adfb-ed45daa86d44"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (50090-3811-0)  / 21 TABLET in 1 BLISTER PACK", "package_ndc": "50090-3811-0", "marketing_start_date": "20181112"}], "brand_name": "methylprednisolone", "product_id": "50090-3811_6bfd8b00-0c6c-40cb-b0dc-677d8d0d0563", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-3811", "generic_name": "methylprednisolone", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "methylprednisolone", "active_ingredients": [{"name": "METHYLPREDNISOLONE", "strength": "4 mg/1"}], "application_number": "ANDA206751", "marketing_category": "ANDA", "marketing_start_date": "20180501", "listing_expiration_date": "20271231"}