methylprednisolone

Generic: methylprednisolone

Labeler: mylan pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

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

methylprednisolone 4 mg/1

Manufacturer
Mylan Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 59762-4440
Product ID 59762-4440_757e97bc-e224-4e63-819b-2f3213428207
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA011153
Listing Expiration 2026-12-31
Marketing Start 2011-10-11

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 597624440
Hyphenated Format 59762-4440

Supplemental Identifiers

RxCUI
197971 197973 259966 328161 762675
UPC
0359762005014 0359762005113 0359762444035
UNII
X4W7ZR7023
NUI
N0000175576 N0000175450

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 (source: ndc)
Generic Name methylprednisolone (source: ndc)
Application Number NDA011153 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 1 DOSE PACK in 1 CARTON (59762-4440-2) / 21 TABLET in 1 DOSE PACK
  • 100 TABLET in 1 BOTTLE (59762-4440-3)
source: ndc

Packages (2)

59762-4440-2 1 DOSE PACK in 1 CARTON (59762-4440-2) / 21 TABLET in 1 DOSE PACK 59762-4440-3 100 TABLET in 1 BOTTLE (59762-4440-3)

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": "757e97bc-e224-4e63-819b-2f3213428207", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0359762005014", "0359762005113", "0359762444035"], "unii": ["X4W7ZR7023"], "rxcui": ["197971", "197973", "259966", "328161", "762675"], "spl_set_id": ["22dd75d6-f89a-44f7-8ca6-b64c4e9806dd"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 DOSE PACK in 1 CARTON (59762-4440-2)  / 21 TABLET in 1 DOSE PACK", "package_ndc": "59762-4440-2", "marketing_start_date": "20111011"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (59762-4440-3)", "package_ndc": "59762-4440-3", "marketing_start_date": "20111011"}], "brand_name": "Methylprednisolone", "product_id": "59762-4440_757e97bc-e224-4e63-819b-2f3213428207", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "59762-4440", "generic_name": "methylprednisolone", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylprednisolone", "active_ingredients": [{"name": "METHYLPREDNISOLONE", "strength": "4 mg/1"}], "application_number": "NDA011153", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20111011", "listing_expiration_date": "20261231"}