NDC codes

FDA NDC Directory
Product NDC (as listed)50090-3094Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-3094Add 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
50090-3094-0500903094005009030940021 TABLET in 1 BLISTER PACK (50090-3094-0)Marketed from Jul 18, 2017

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)
Methylprednisolone
Generic name (nonproprietary)
methylprednisolone
Active ingredients
Methylprednisolone — 4 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 040189
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 50090-3094_3d2362f8-b64d-417d-9dab-66d7de2c1b0aSPL ID 3d2362f8-b64d-417d-9dab-66d7de2c1b0aSPL set ID eb479561-142d-410c-84b2-988375c6a96eRxCUI 259966, 762675UNII X4W7ZR7023
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

N450090309400 followed by a unit qualifier and the quantity

Package 50090-3094-00. 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 AND USAGE Methylprednisolone Tablets are indicated in the following conditions: 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: Rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require l…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50090-3094

What is NDC 50090-3094?
50090-3094 is the product NDC for Methylprednisolone, Methylprednisolone 4 mg/1 tablet, listed with the FDA by A-S Medication Solutions. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Methylprednisolone.
What is the active ingredient?
Methylprednisolone.
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 Methylprednisolone?
48 other product NDCs are listed under this name. See all Methylprednisolone 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 Methylprednisolone NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
methylprednisoloneMethylprednisolone 4 mg/1TabletOralBluePoint Laboratories68001-62468001-0624-01
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralREMEDYREPACK INC.70518-421370518-4213-00
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-96160760-0961-21
methylprednisoloneMethylprednisolone 4 mg/1TabletOralREMEDYREPACK INC.70518-362270518-3622-01
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-023080425-0230-01
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-023180425-0231-01
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-025580425-0255-01
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralDirect_Rx72189-26472189-0264-21
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-783368788-7833-02
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralREMEDYREPACK INC.70518-286470518-2864-00

All 49 Methylprednisolone NDCs

Other NDCs under ANDA 040189

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

FDA NDC Directory listings under ANDA 040189
ProductStrengthForm · routeLabelerProduct NDC
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralProficient Rx LP63187-160
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralAsclemed USA, Inc.76420-041
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0230

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