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NDC 00009-0022-01 Medrol 8 mg/1 Details
Medrol 8 mg/1
Medrol is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Pharmacia & Upjohn Company LLC. The primary component is METHYLPREDNISOLONE.
MedlinePlus Drug Summary
Methylprednisolone, a corticosteroid, is similar to a natural hormone produced by your adrenal glands. It is often used to replace this chemical when your body does not make enough of it. It relieves inflammation (swelling, heat, redness, and pain) and is used to treat certain forms of arthritis; skin, blood, kidney, eye, thyroid, and intestinal disorders (e.g., colitis); severe allergies; and asthma. Methylprednisolone is also used to treat certain types of cancer. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
Related Packages: 00009-0022-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Methylprednisolone
Product Information
| NDC | 00009-0022 |
|---|---|
| Product ID | 0009-0022_9f1ff5b5-f68d-43cf-af32-3e0db5ec3eba |
| Associated GPIs | 22100030000315 |
| GCN Sequence Number | 006742 |
| GCN Sequence Number Description | methylprednisolone TABLET 8 MG ORAL |
| HIC3 | P5A |
| HIC3 Description | GLUCOCORTICOIDS |
| GCN | 27058 |
| HICL Sequence Number | 002877 |
| HICL Sequence Number Description | METHYLPREDNISOLONE |
| Brand/Generic | Brand |
| Proprietary Name | Medrol |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | methylprednisolone |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 8 |
| Active Ingredient Units | mg/1 |
| Substance Name | METHYLPREDNISOLONE |
| Labeler Name | Pharmacia & Upjohn Company LLC |
| Pharmaceutical Class | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
| DEA Schedule | n/a |
| Marketing Category | NDA |
| Application Number | NDA011153 |
| Listing Certified Through | 2025-12-31 |
Package
NDC 00009-0022-01 (00009002201)
| NDC Package Code | 0009-0022-01 |
|---|---|
| Billing NDC | 00009002201 |
| Package | 25 TABLET in 1 BOTTLE (0009-0022-01) |
| Marketing Start Date | 1957-10-24 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |