Prednisone NDC 0603-5337

Product information

Brand name (proprietary)

Prednisone

Generic name (nonproprietary)

prednisone

Active ingredients

Prednisone — 5 mg/1

Dosage form

Tablet

Route

Oral

Labeler

Par Health USA, LLC

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 040256

Marketing start

Jul 12, 2002

Listing expires

Dec 31, 2027

Other FDA classes

Corticosteroid Hormone Receptor Agonists (Mechanism)

Identifiers

Product ID 0603-5337_68bdeba1-553d-4d18-ae66-5eb8a0a880b8SPL ID 68bdeba1-553d-4d18-ae66-5eb8a0a880b8SPL set ID 10fe5a3b-84dc-4600-87c2-b80c97ce18cfRxCUI 198144, 198145, 198146, 312615, 312617, 763179, 763181, 763183, 763185UNII VB0R961HZTUPC 0306035338317, 0306035337211, 0306035338157, 0306035335217, 0306035336214, 0306035337310, 0306035338218

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

N400603533715 followed by a unit qualifier and the quantity Copy

Package 00603-5337-15. 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 040256

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