What is NDC 17856-3722?

17856-3722 is the product NDC for PredniSONE, Prednisone 5 mg/5mL solution, listed with the FDA by Atlantic Biologicals Corps. It has 3 package NDCs, shown above in 10- and 11-digit form.

Atlantic Biologicals Corps, NDC labeler code 17856. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for PredniSONE?

281 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

PredniSONE NDC 17856-3722 | National Drug Code

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	1785637220117856372201	5 mL in 1 CUP (17856-3722-1)Marketed from May 5, 2016
17856-3722-2	1785637220217856372202	45 SYRINGE in 1 CASE (17856-3722-2) / 5 mL in 1 SYRINGEMarketed from Sep 17, 2026
17856-3722-3	1785637220317856372203	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 CorpsNDC labeler code 17856
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_5ca0f140-733f-3765-e063-6394a90a3df6SPL ID 5ca0f140-733f-3765-e063-6394a90a3df6
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.

About NDC 17856-3722

What is NDC 17856-3722?: 17856-3722 is the product NDC for PredniSONE, Prednisone 5 mg/5mL solution, listed with the FDA by Atlantic Biologicals Corps. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: PredniSONE.
What is the active ingredient?: Prednisone.
Who is the labeler?: Atlantic Biologicals Corps, NDC labeler code 17856. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for PredniSONE?: 281 other product NDCs are listed under this name. See all PredniSONE NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other PredniSONE NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
PredniSONE	Prednisone 10 mg/1	TabletOral	Coupler LLC	67046-1294	67046-1294-03
PredniSONE	Prednisone 20 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4182	68788-4182-0168788-4182-0268788-4182-03+3 more
prednisone	Prednisone 10 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-069	87441-0069-01
prednisone	Prednisone 50 mg/1	TabletOral	Coupler LLC	67046-1171	67046-1171-03
prednisone	Prednisone 5 mg/1	TabletOral	Cardinal Health 107, LLC	55154-2582	55154-2582-00
prednisone	Prednisone 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4660	70518-4660-00
Prednisone	Prednisone 50 mg/1	TabletOral	Coupler LLC	67046-1379	67046-1379-03
Prednisone	Prednisone 20 mg/1	TabletOral	Cardinal Health 107, LLC	55154-2581	55154-2581-00
Prednisone	Prednisone 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4560	70518-4560-00
prednisone	Prednisone 5 mg/1	TabletOral	American Health Packaging	60687-903	60687-0903-01

All 282 PredniSONE NDCs

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