Prescription drug · NDA
Medrol (Methylprednisolone) NDC 0009-0022
Methylprednisolone 8 mg/1 · Tablet · Oral · Pharmacia & Upjohn Company LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0009-0022-01 | 0000900220100009002201 | 25 TABLET in 1 BOTTLE (0009-0022-01)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 — 8 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Pharmacia & Upjohn Company LLCNDC labeler code 0009
- 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 0009-0022_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
N400009002201followed by a unit qualifier and the quantityPackage 00009-0022-01. 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.
About NDC 0009-0022
- What is NDC 0009-0022?
- 0009-0022 is the product NDC for Medrol (methylprednisolone), Methylprednisolone 8 mg/1 tablet, listed with the FDA by Pharmacia & Upjohn Company LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Medrol (Methylprednisolone).
- What is the active ingredient?
- Methylprednisolone.
- Who is the labeler?
- Pharmacia & Upjohn Company LLC, NDC labeler code 0009. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Medrol?
- 3 other product NDCs are listed under this name. See all Medrol NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Medrol products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Medrolmethylprednisolone | Methylprednisolone 2 mg/1 | TabletOral | Pharmacia & Upjohn Company LLC | 0009-0020 | 00009-0020-01 |
| Medrolmethylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | Pharmacia & Upjohn Company LLC | 0009-0056 | 00009-0056-0200009-0056-04 |
| Medrolmethylprednisolone | Methylprednisolone 16 mg/1 | TabletOral | Pharmacia & Upjohn Company LLC | 0009-0073 | 00009-0073-01 |
Other NDCs under NDA 011153
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | REMEDYREPACK INC. | 70518-4213 |
| Methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | NuCare Pharmaceuticals,Inc. | 68071-2370 |
| Methylprednisolone | Methylprednisolone 16 mg/1 | TabletOral | Mylan Pharmaceuticals Inc. | 59762-0050 |
| Methylprednisolone | Methylprednisolone 8 mg/1 | TabletOral | Mylan Pharmaceuticals Inc. | 59762-0049 |
| Methylprednisolone | Methylprednisolone 32 mg/1 | TabletOral | Mylan Pharmaceuticals Inc. | 59762-0051 |
| Medrolmethylprednisolone | Methylprednisolone 16 mg/1 | TabletOral | Pharmacia & Upjohn Company LLC | 0009-0073 |
| Medrolmethylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | Pharmacia & Upjohn Company LLC | 0009-0056 |
| Medrolmethylprednisolone | Methylprednisolone 2 mg/1 | TabletOral | Pharmacia & Upjohn Company LLC | 0009-0020 |
| Methylprednisolone | Methylprednisolone 4 mg/1 | TabletOral | Mylan Pharmaceuticals Inc. | 59762-4440 |