What is NDC 87063-048?

87063-048 is the product NDC for Prednisone, Prednisone 50 mg/1 tablet, listed with the FDA by ASCLEMED USA INC.. It has 8 package NDCs, shown above in 10- and 11-digit form.

ASCLEMED USA INC., NDC labeler code 87063. 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?

282 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 87063-048 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)87063-048Labeler and product segments. Claims need a package NDC.

Product NDC at billing width87063-0048Add 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
87063-048-01	87063004801	100 TABLET in 1 BOTTLE (87063-048-01)Marketed from Dec 3, 2025
87063-048-18	87063004818	18 TABLET in 1 BOTTLE (87063-048-18)Marketed from Dec 3, 2025
87063-048-20	87063004820	20 TABLET in 1 BOTTLE (87063-048-20)Marketed from Dec 3, 2025
87063-048-21	87063004821	21 TABLET in 1 BOTTLE (87063-048-21)Marketed from Dec 3, 2025
87063-048-30	87063004830	30 TABLET in 1 BOTTLE (87063-048-30)Marketed from Dec 3, 2025
87063-048-60	87063004860	60 TABLET in 1 BOTTLE (87063-048-60)Marketed from Dec 3, 2025
87063-048-78	87063004878	10 BLISTER PACK in 1 CARTON (87063-048-78) / 10 TABLET in 1 BLISTER PACKMarketed from Dec 3, 2025
87063-048-90	87063004890	90 TABLET in 1 BOTTLE (87063-048-90)Marketed from Dec 3, 2025

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 — 50 mg/1
Dosage form: Tablet
Route: Oral
Labeler: ASCLEMED USA INC.NDC labeler code 87063
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 215672
Marketing start: Mar 28, 2022
Listing expires: Dec 31, 2027
Other FDA classes: Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers: Product ID 87063-048_4a1001c0-0013-e6a5-e063-6294a90af48eSPL ID 4a1001c0-0013-e6a5-e063-6294a90af48eSPL set ID bf6ebe58-e7bb-49d3-842e-3372f8ba6172RxCUI 198145, 198146, 198148, 312615, 312617UNII 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

N487063004801 followed by a unit qualifier and the quantity

Package 87063-0048-01. 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

Current FDA label (SPL), effective Feb 5, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Prednisone tablets 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 re…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 87063-048

What is NDC 87063-048?: 87063-048 is the product NDC for Prednisone, Prednisone 50 mg/1 tablet, listed with the FDA by ASCLEMED USA INC.. It has 8 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?: ASCLEMED USA INC., NDC labeler code 87063. 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?: 282 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 283 Prednisone NDCs

Other NDCs under ANDA 215672

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

FDA NDC Directory listings under ANDA 215672
Product	Strength	Form · route	Labeler	Product NDC
Prednisone	Prednisone 10 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3746
Prednisone	Prednisone 20 mg/1	TabletOral	Coupler LLC	67046-1610
Prednisone	Prednisone 20 mg/1	TabletOral	A-S Medication Solutions	50090-8087
Prednisone	Prednisone 20 mg/1	TabletOral	A-S Medication Solutions	50090-8083
Prednisone	Prednisone 20 mg/1	TabletOral	A-S Medication Solutions	50090-8084
Prednisone	Prednisone 50 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-426
Prednisone	Prednisone 2.5 mg/1	TabletOral	A-S Medication Solutions	50090-7825
Prednisone	Prednisone 5 mg/1	TabletOral	Advanced Rx of Tennessee, LLC	80425-0479
Prednisone	Prednisone 50 mg/1	TabletOral	Coupler LLC	67046-1379
Prednisone	Prednisone 2.5 mg/1	TabletOral	Bryant Ranch Prepack	71335-2356
Prednisone	Prednisone 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-4243
Prednisone	Prednisone 20 mg/1	TabletOral	QPharma, Inc.	42708-195
Prednisone	Prednisone 5 mg/1	TabletOral	A-S Medication Solutions	50090-7935
Prednisone	Prednisone 5 mg/1	TabletOral	A-S Medication Solutions	50090-7931
Prednisone	Prednisone 5 mg/1	TabletOral	A-S Medication Solutions	50090-7933
Prednisone	Prednisone 50 mg/1	TabletOral	Bryant Ranch Prepack	71335-2389
Prednisone	Prednisone 10 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3641
Prednisone	Prednisone 20 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8819
Prednisone	Prednisone 20 mg/1	TabletOral	Redpharm Drug	67296-2182
Prednisone	Prednisone 2.5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8858

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