methylprednisolone

Generic: methylprednisolone

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

Drug Facts

Product Profile

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

methylprednisolone 4 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4213
Product ID 70518-4213_3ff680c9-1eea-146b-e063-6394a90a7fa7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA011153
Listing Expiration 2026-12-31
Marketing Start 2024-10-14

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 705184213
Hyphenated Format 70518-4213

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 NDA011153 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 1 DOSE PACK in 1 CARTON (70518-4213-0) / 21 TABLET in 1 DOSE 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": "3ff680c9-1eea-146b-e063-6394a90a7fa7", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["X4W7ZR7023"], "rxcui": ["259966", "762675"], "spl_set_id": ["d2a0e52c-f724-40e6-9d2a-5f1487c104b6"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 DOSE PACK in 1 CARTON (70518-4213-0)  / 21 TABLET in 1 DOSE PACK", "package_ndc": "70518-4213-0", "marketing_start_date": "20241014"}], "brand_name": "Methylprednisolone", "product_id": "70518-4213_3ff680c9-1eea-146b-e063-6394a90a7fa7", "dosage_form": "TABLET", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70518-4213", "generic_name": "methylprednisolone", "labeler_name": "REMEDYREPACK 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": "20241014", "listing_expiration_date": "20261231"}