What is NDC 72189-589?

72189-589 is the product NDC for Prednisone, Prednisone 10 mg/1 tablet, listed with the FDA by Direct_Rx. It has 4 package NDCs, shown above in 10- and 11-digit form.

Direct_Rx, NDC labeler code 72189. 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?

280 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 72189-589 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)72189-589Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72189-0589Add 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
72189-589-10	72189058910	10 TABLET in 1 BOTTLE (72189-589-10)Marketed from Oct 15, 2024
72189-589-15	72189058915	15 TABLET in 1 BOTTLE (72189-589-15)Marketed from Oct 15, 2024
72189-589-21	72189058921	21 TABLET in 1 BOTTLE (72189-589-21)Marketed from Oct 15, 2024
72189-589-30	72189058930	30 TABLET in 1 BOTTLE (72189-589-30)Marketed from Oct 15, 2024

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: Direct_RxNDC labeler code 72189
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208412
Marketing start: Oct 15, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 72189-589_410c34bc-cd00-f063-e063-6394a90aa7f6SPL ID 410c34bc-cd00-f063-e063-6394a90aa7f6SPL set ID 24882e23-c05f-f2ee-e063-6294a90a536fRxCUI 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

N472189058910 followed by a unit qualifier and the quantity

Package 72189-0589-10. 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

Current FDA label (SPL), effective Oct 13, 2025.

Indications (excerpt from the label)

Prednisone tablets USP are indicated in the following conditions: Endocrine Disorders Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the first choice: synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy mineralocorticoid supplementation is of particular importance); congenital adrenal hyperplasia; hypercalcemia associated with cancer; nonsuppurative thyroiditis. Rheumatic Disorders As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in: psoriatic arthritis, rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dos…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72189-589

What is NDC 72189-589?: 72189-589 is the product NDC for Prednisone, Prednisone 10 mg/1 tablet, listed with the FDA by Direct_Rx. It has 4 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?: Direct_Rx, NDC labeler code 72189. 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?: 280 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 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
prednisone	Prednisone 5 mg/1	TabletOral	Coupler LLC	67046-1642	67046-1642-03

All 281 Prednisone NDCs

Other NDCs under ANDA 208412

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

FDA NDC Directory listings under ANDA 208412
Product	Strength	Form · route	Labeler	Product NDC
prednisone	Prednisone 10 mg/1	TabletOral	QPharma Inc	42708-166
prednisone	Prednisone 5 mg/1	TabletOral	QPharma Inc	42708-186
prednisone	Prednisone 20 mg/1	TabletOral	Medsource Pharmaceuticals	45865-884
prednisone	Prednisone 50 mg/1	TabletOral	A-S Medication Solutions	50090-6376
prednisone	Prednisone 10 mg/1	TabletOral	A-S Medication Solutions	50090-7218
prednisone	Prednisone 10 mg/1	TabletOral	A-S Medication Solutions	50090-7219
prednisone	Prednisone 5 mg/1	TabletOral	A-S Medication Solutions	50090-7505
prednisone	Prednisone 20 mg/1	TabletOral	A-S Medication Solutions	50090-8051
prednisone	Prednisone 20 mg/1	TabletOral	A-S Medication Solutions	50090-8052
prednisone	Prednisone 50 mg/1	TabletOral	Northwind Health Company, LLC	51655-349
prednisone	Prednisone 20 mg/1	TabletOral	Northwind Health Company, LLC	51655-541
prednisone	Prednisone 10 mg/1	TabletOral	Northwind Health Company, LLC	51655-972
Prednisone	Prednisone 20 mg/1	TabletOral	Cardinal Health 107, LLC	55154-2581
prednisone	Prednisone 5 mg/1	TabletOral	Cardinal Health 107, LLC	55154-2582
Prednisone	Prednisone 50 mg/1	TabletOral	American Health Packaging	60687-854
prednisone	Prednisone 5 mg/1	TabletOral	American Health Packaging	60687-903
Prednisone	Prednisone 10 mg/1	TabletOral	American Health Packaging	60687-914
Prednisone	Prednisone 20 mg/1	TabletOral	American Health Packaging	60687-925
prednisone	Prednisone 20 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-790
prednisone	Prednisone 5 mg/1	TabletOral	Strides Pharma Science Limited	64380-783

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