Methylprednisolone
- Product NDC
- 50436-0001
- 11-digit product format
- 504360001
- Labeler code
- 50436
- Product ID
- 50436-0001_9c9eb3ea-c5df-4f8e-838f-a789e98a8743
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA040189
- Marketing category
- ANDA
- Marketing start
- 1997-10-31
- Marketing end
- 0000-00-00
- Substance
- METHYLPREDNISOLONE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-0001-1 | Methylprednisolone | 21 in 1 BOTTLE | TABLET | 21 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0001 | METHYLPREDNISOLONE (METHYLPREDNISOLONE) TABLET [UNIT DOSE SERVICES] | 2 | Legacy NDC, 1 package rows | 20210919_b3139a6a-e9dd-4aeb-9d69-ed98941cf28e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50436-0001-1 | 50436000101 | 21 TABLET in 1 BOTTLE (50436-0001-1) | 21 tablet | 2021-09-17 | 0000-00-00 | No | No | Current |