NDC codes

FDA NDC Directory
Product NDC (as listed)50090-8084Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-8084Add 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
50090-8084-05009080840020 TABLET in 1 BOTTLE (50090-8084-0)Marketed from Sep 21, 2026
50090-8084-15009080840112 TABLET in 1 BOTTLE (50090-8084-1)Marketed from Sep 21, 2026
50090-8084-2500908084026 TABLET in 1 BOTTLE (50090-8084-2)Marketed from Sep 21, 2026
50090-8084-55009080840514 TABLET in 1 BOTTLE (50090-8084-5)Marketed from Sep 21, 2026
50090-8084-75009080840715 TABLET in 1 BOTTLE (50090-8084-7)Marketed from Sep 21, 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 — 20 mg/1
Dosage form
Tablet
Route
Oral
Labeler
A-S Medication SolutionsNDC labeler code 50090
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215672
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 50090-8084_442aada1-ed52-492e-b706-8f9adf1e48abSPL ID 442aada1-ed52-492e-b706-8f9adf1e48ab
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

N450090808400 followed by a unit qualifier and the quantity

Package 50090-8084-00. 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

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

About NDC 50090-8084

What is NDC 50090-8084?
50090-8084 is the product NDC for Prednisone, Prednisone 20 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 5 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?
A-S Medication Solutions, NDC labeler code 50090. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
PredniSONEPrednisone 20 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-418268788-4182-0168788-4182-0268788-4182-03+3 more
prednisonePrednisone 10 mg/1TabletOralUnit Dose Solutions, Inc.87441-06987441-0069-01
prednisonePrednisone 50 mg/1TabletOralCoupler LLC67046-117167046-1171-03
prednisonePrednisone 5 mg/1TabletOralCardinal Health 107, LLC55154-258255154-2582-00
prednisonePrednisone 10 mg/1TabletOralREMEDYREPACK INC.70518-466070518-4660-00
PrednisonePrednisone 50 mg/1TabletOralCoupler LLC67046-137967046-1379-03
PrednisonePrednisone 20 mg/1TabletOralCardinal Health 107, LLC55154-258155154-2581-00
PrednisonePrednisone 10 mg/1TabletOralREMEDYREPACK INC.70518-456070518-4560-00
prednisonePrednisone 5 mg/1TabletOralAmerican Health Packaging60687-90360687-0903-01
prednisonePrednisone 5 mg/1TabletOralCoupler LLC67046-164267046-1642-03

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
ProductStrengthForm · routeLabelerProduct NDC
PrednisonePrednisone 10 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3746
PrednisonePrednisone 20 mg/1TabletOralCoupler LLC67046-1610
PrednisonePrednisone 20 mg/1TabletOralA-S Medication Solutions50090-8087
PrednisonePrednisone 20 mg/1TabletOralA-S Medication Solutions50090-8083
PrednisonePrednisone 50 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-426
PrednisonePrednisone 2.5 mg/1TabletOralA-S Medication Solutions50090-7825
PrednisonePrednisone 5 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0479
PrednisonePrednisone 50 mg/1TabletOralCoupler LLC67046-1379
PrednisonePrednisone 2.5 mg/1TabletOralBryant Ranch Prepack71335-2356
PrednisonePrednisone 20 mg/1TabletOralREMEDYREPACK INC.70518-4243
PrednisonePrednisone 20 mg/1TabletOralQPharma, Inc.42708-195
PrednisonePrednisone 5 mg/1TabletOralA-S Medication Solutions50090-7935
PrednisonePrednisone 5 mg/1TabletOralA-S Medication Solutions50090-7931
PrednisonePrednisone 5 mg/1TabletOralA-S Medication Solutions50090-7933
PrednisonePrednisone 50 mg/1TabletOralBryant Ranch Prepack71335-2389
PrednisonePrednisone 10 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3641
PrednisonePrednisone 20 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8819
PrednisonePrednisone 20 mg/1TabletOralRedpharm Drug67296-2182
PrednisonePrednisone 2.5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8858
PrednisonePrednisone 2.5 mg/1TabletOralASCLEMED USA INC.87063-042

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