NDC codes

FDA NDC Directory
Product NDC (as listed)59762-0049Labeler and product segments. Claims need a package NDC.
Product NDC at billing width59762-0049Add 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
59762-0049-15976200490125 TABLET in 1 BOTTLE (59762-0049-1)Marketed from Mar 25, 2013

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 — 8 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 011153
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 59762-0049_bc3419a0-22a3-4eaf-a4f2-3133e9380663SPL ID bc3419a0-22a3-4eaf-a4f2-3133e9380663SPL set ID 22dd75d6-f89a-44f7-8ca6-b64c4e9806ddRxCUI 197971, 197973, 259966, 328161, 762675UNII X4W7ZR7023UPC 0359762005014, 0359762005113, 0359762444035
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

N459762004901 followed by a unit qualifier and the quantity

Package 59762-0049-01. 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 .

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 requir…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 011153

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

FDA NDC Directory listings under NDA 011153
ProductStrengthForm · routeLabelerProduct NDC
MedrolmethylprednisoloneMethylprednisolone 16 mg/1TabletOralPharmacia & Upjohn Company LLC0009-0073
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2370
MedrolmethylprednisoloneMethylprednisolone 4 mg/1TabletOralPharmacia & Upjohn Company LLC0009-0056
MedrolmethylprednisoloneMethylprednisolone 2 mg/1TabletOralPharmacia & Upjohn Company LLC0009-0020
MethylprednisoloneMethylprednisolone 32 mg/1TabletOralMylan Pharmaceuticals Inc.59762-0051
MedrolmethylprednisoloneMethylprednisolone 8 mg/1TabletOralPharmacia & Upjohn Company LLC0009-0022
MethylprednisoloneMethylprednisolone 16 mg/1TabletOralMylan Pharmaceuticals Inc.59762-0050
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralMylan Pharmaceuticals Inc.59762-4440
MethylprednisoloneMethylprednisolone 4 mg/1TabletOralREMEDYREPACK INC.70518-4213

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Methylprednisolone NDC 59762-0049 | Med-Code