NDC codes

FDA NDC Directory
Product NDC (as listed)50090-7684Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-7684Add 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 NDC11-digit (billing)PackageCopy
50090-7684-05009076840021 TABLET in 1 BOTTLE (50090-7684-0)Marketed from Oct 9, 2025
50090-7684-15009076840150 TABLET in 1 BOTTLE (50090-7684-1)Marketed from Oct 9, 2025
50090-7684-350090768403100 TABLET in 1 BOTTLE (50090-7684-3)Marketed from Oct 9, 2025
50090-7684-45009076840430 TABLET in 1 BOTTLE (50090-7684-4)Marketed from Oct 9, 2025
50090-7684-75009076840760 TABLET in 1 BOTTLE (50090-7684-7)Marketed from Oct 9, 2025

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/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213385
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 50090-7684_4e631e86-7caf-4cad-8d38-f24c5d1d968bSPL ID 4e631e86-7caf-4cad-8d38-f24c5d1d968bSPL set ID 43a4b2eb-f2cd-410f-9719-577fdc4ad5deRxCUI 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

N450090768400 followed by a unit qualifier and the quantity

Package 50090-7684-00. 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 .

Indications (excerpt from the label)

INDICATIONS 1. 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 Nonsuppurative thyroiditis Hypercalcemia associated with cancer 2. 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-dose maintenance therapy) Ankylosing spondylitis Acute a…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 213385

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

FDA NDC Directory listings under ANDA 213385
ProductStrengthForm · routeLabelerProduct NDC
prednisonePrednisone 5 mg/1TabletOralNorthwind Health Company, LLC51655-988
prednisonePrednisone 5 mg/1TabletOralA-S Medication Solutions50090-7686
prednisonePrednisone 5 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8439
prednisonePrednisone 5 mg/1TabletOralA-S Medication Solutions50090-7688
prednisonePrednisone 1 mg/1TabletOralAmneal Pharmaceuticals NY LLC60219-1705
prednisonePrednisone 5 mg/1TabletOralAmneal Pharmaceuticals NY LLC60219-1706

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