prednisone NDC 71205-818

Product information

Brand name (proprietary)

prednisone

Generic name (nonproprietary)

prednisone

Active ingredients

Prednisone — 10 mg/1

Dosage form

Tablet

Route

Oral

Labeler

Proficient Rx LP

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 213386

Marketing start

Jun 24, 2020

Listing expires

Dec 31, 2026

Other FDA classes

Corticosteroid Hormone Receptor Agonists (Mechanism)

Identifiers

Product ID 71205-818_6ec5b58c-65e9-47ee-b2ac-7d0b395a0630SPL ID 6ec5b58c-65e9-47ee-b2ac-7d0b395a0630SPL set ID 6ec5b58c-65e9-47ee-b2ac-7d0b395a0630RxCUI 198145UNII VB0R961HZTUPC 0371205818210

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 HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N471205081805 followed by a unit qualifier and the quantity Copy

Package 71205-0818-05. 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

Other NDCs under ANDA 213386

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