PredniSONE NDC 17856-3722

NDC codes

FDA NDC Directory

Product NDC (as listed)17856-3722Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17856-3722Add 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
17856-3722-1	17856372201	5 mL in 1 CUP (17856-3722-1)Marketed from May 5, 2016
17856-3722-2	17856372202	45 SYRINGE in 1 CASE (17856-3722-2) / 5 mL in 1 SYRINGEMarketed from Sep 17, 2026
17856-3722-3	17856372203	45 SYRINGE in 1 CASE (17856-3722-3) / 5 mL in 1 SYRINGEMarketed from Sep 17, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — 5 mg/5mL
Dosage form: Solution
Route: Oral
Labeler: Atlantic Biologicals Corps
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 088703
Marketing start: Dec 13, 1986
Listing expires: Dec 31, 2027
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 17856-3722_5baf5a69-3431-f2ff-e063-6394a90af439SPL ID 5baf5a69-3431-f2ff-e063-6394a90af439
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

N417856372201 followed by a unit qualifier and the quantity

Package 17856-3722-01. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 088703

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

FDA NDC Directory listings under ANDA 088703
Product	Strength	Form · route	Labeler	Product NDC
PredniSONE	Prednisone 5 mg/5mL	SolutionOral	Hikma Pharmaceuticals USA Inc.	0054-3722