methylprednisolone

Generic: methylprednisolone

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methylprednisolone
Generic Name methylprednisolone
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methylprednisolone 32 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-763
Product ID 62135-763_225669c1-9479-52eb-e063-6394a90a649b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209097
Listing Expiration 2026-12-31
Marketing Start 2019-02-22

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 62135763
Hyphenated Format 62135-763

Supplemental Identifiers

RxCUI
197969 197971 197973 259966 328161
UPC
0362135763268 0362135760212 0362135761264 0362135762506 0362135760014 0362135759308
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 ANDA209097 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 32 mg/1
source: ndc
Packaging
  • 25 TABLET in 1 BOTTLE (62135-763-26)
source: ndc

Packages (1)

62135-763-26 25 TABLET in 1 BOTTLE (62135-763-26)

Ingredients (1)

methylprednisolone (32 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": "225669c1-9479-52eb-e063-6394a90a649b", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0362135763268", "0362135760212", "0362135761264", "0362135762506", "0362135760014", "0362135759308"], "unii": ["X4W7ZR7023"], "rxcui": ["197969", "197971", "197973", "259966", "328161"], "spl_set_id": ["bdd048bb-7e6c-45c7-b51a-075e83ca9f5b"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 TABLET in 1 BOTTLE (62135-763-26)", "package_ndc": "62135-763-26", "marketing_start_date": "20240514"}], "brand_name": "Methylprednisolone", "product_id": "62135-763_225669c1-9479-52eb-e063-6394a90a649b", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "62135-763", "generic_name": "Methylprednisolone", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylprednisolone", "active_ingredients": [{"name": "METHYLPREDNISOLONE", "strength": "32 mg/1"}], "application_number": "ANDA209097", "marketing_category": "ANDA", "marketing_start_date": "20190222", "listing_expiration_date": "20261231"}