methylprednisolone

Generic: methylprednisolone

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methylprednisolone
Generic Name methylprednisolone
Labeler direct_rx
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methylprednisolone 4 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-264
Product ID 72189-264_2c28f93c-99a2-f643-e063-6394a90a6f9d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204072
Listing Expiration 2026-12-31
Marketing Start 2021-09-13

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 72189264
Hyphenated Format 72189-264

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 ANDA204072 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 21 TABLET in 1 BOTTLE (72189-264-21)
source: ndc

Packages (1)

72189-264-21 21 TABLET in 1 BOTTLE (72189-264-21)

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": "2c28f93c-99a2-f643-e063-6394a90a6f9d", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["X4W7ZR7023"], "rxcui": ["259966", "762675"], "spl_set_id": ["8c3f3f63-8a05-7a4a-e053-2995a90ad95a"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE (72189-264-21)", "package_ndc": "72189-264-21", "marketing_start_date": "20210913"}], "brand_name": "METHYLPREDNISOLONE", "product_id": "72189-264_2c28f93c-99a2-f643-e063-6394a90a6f9d", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72189-264", "generic_name": "METHYLPREDNISOLONE", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHYLPREDNISOLONE", "active_ingredients": [{"name": "METHYLPREDNISOLONE", "strength": "4 mg/1"}], "application_number": "ANDA204072", "marketing_category": "ANDA", "marketing_start_date": "20210913", "listing_expiration_date": "20261231"}