PredniSONE NDC 51655-493

NDC codes

FDA NDC Directory

Product NDC (as listed)51655-493Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51655-0493Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
51655-493-49	51655049349	42 TABLET in 1 BOTTLE, PLASTIC (51655-493-49)Marketed from Jan 13, 2021

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): PredniSONE
Generic name (nonproprietary): prednisone
Active ingredients: Prednisone — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Northwind Health Company, LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 084122
Marketing start: Jan 13, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 51655-493_490f89bb-255b-5669-e063-6394a90a4a53SPL ID 490f89bb-255b-5669-e063-6394a90a4a53SPL set ID dad4f191-8893-48e0-e053-2995a90ae864RxCUI 198145UNII VB0R961HZT
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

N451655049349 followed by a unit qualifier and the quantity

Package 51655-0493-49. 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 084122

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

FDA NDC Directory listings under ANDA 084122
Product	Strength	Form · route	Labeler	Product NDC
PredniSONE	Prednisone 10 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0485
PredniSONE	Prednisone 10 mg/1	TabletOral	QPharma, Inc.	42708-045
PredniSONE	Prednisone 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4191