Methylprednisolone Sodium Succinate NDC 82094-401

Product information

Brand name (proprietary)

Methylprednisolone Sodium Succinate

Generic name (nonproprietary)

methylprednisolone

Active ingredients

Methylprednisolone sodium succinate — 40 mg/mL

Dosage form

Injection, Powder, Lyophilized, For solution

Route

Intramuscular, Intravenous

Labeler

Tianjin Kingyork Pharmaceuticals Co., Ltd

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 212396

Marketing start

Apr 20, 2021

Listing expires

Dec 31, 2026

Other FDA classes

Corticosteroid Hormone Receptor Agonists (Mechanism)

Identifiers

Product ID 82094-401_94c8ce6b-7622-4d1f-8b54-0ce959752ae5SPL ID 94c8ce6b-7622-4d1f-8b54-0ce959752ae5SPL set ID 77a8d96c-37df-4f3a-9757-b2d4131ff82bRxCUI 311659, 314099, 1357886, 1743704UNII LEC9GKY20K

Pharmacologic class

Corticosteroid

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N482094040150 followed by a unit qualifier and the quantity Copy

Package 82094-0401-50. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 212396

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.