NDC codes

FDA NDC Directory
Product NDC (as listed)0009-0073Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00009-0073Add 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
0009-0073-010000900730150 TABLET in 1 BOTTLE (0009-0073-01)Marketed from Oct 24, 1957

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Medrol
Generic name (nonproprietary)
methylprednisolone
Active ingredients
Methylprednisolone — 16 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 011153
Marketing start
Listing expires
Other FDA classes
Corticosteroid Hormone Receptor Agonists (Mechanism)
Identifiers
Product ID 0009-0073_e4a8e5b4-af77-4eca-92de-cd0982969b82SPL ID e4a8e5b4-af77-4eca-92de-cd0982969b82SPL set ID 39d5270b-d957-4821-93d6-501b7b9f02d4RxCUI 197969, 197971, 197973, 207136, 207137, 207138, 207141, 259966, 260330, 328161, 762675, 834023UNII X4W7ZR7023UPC 0300090056025, 0300090022013, 0300090073015, 0300090020019
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

N400009007301 followed by a unit qualifier and the quantity

Package 00009-0073-01. 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 MEDROL 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 low-dose ma…

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
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
MethylprednisoloneMethylprednisolone 8 mg/1TabletOralMylan Pharmaceuticals Inc.59762-0049
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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