Methylprednisolone
- Product NDC
- 50090-3094
- 11-digit product format
- 500903094
- Labeler code
- 50090
- Product ID
- 50090-3094_3d2362f8-b64d-417d-9dab-66d7de2c1b0a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040189
- Marketing category
- ANDA
- Marketing start
- 1997-10-31
- Substance
- METHYLPREDNISOLONE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Methylprednisolone
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| METHYLPREDNISOLONE | 4 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | X4W7ZR7023 |
| Rxcui | 259966, 762675 |
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 |
|---|
| 50090-3094-0 | Methylprednisolone | 21 in 1 BLISTER PACK | TABLET | 21 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3094 | METHYLPREDNISOLONE (METHYLPREDNISOLONE) TABLET [A-S MEDICATION SOLUTIONS] | 9 | Current NDC, Legacy NDC, 1 package rows | 20241004_eb479561-142d-410c-84b2-988375c6a96e.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 |
|---|
| 50090-3094-0 | 50090309400 | 21 TABLET in 1 BLISTER PACK (50090-3094-0) | 21 tablet | 2017-07-18 | 0000-00-00 | No | No | Current |