methylprednisolone
- Product NDC
- 68001-624
- 11-digit product format
- 680010624
- Labeler code
- 68001
- Product ID
- 68001-624_5267c1af-043e-c1e6-e063-6294a90a42d1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA206751
- Marketing category
- ANDA
- Marketing start
- 2025-05-01
- Substance
- METHYLPREDNISOLONE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- methylprednisolone
- Listing expiration
- 2027-12-31
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#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68001-624-01 | methylprednisolone | 21 in 1 BLISTER PACK | TABLET | 21 | | 3 |
| 68001-624-01 | methylprednisolone | 1 in 1 CARTON | TABLET | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68001-624 | METHYLPREDNISOLONE TABLET [BLUEPOINT LABORATORIES] | 1 | Current NDC, 2 package rows | 20250502_7092df48-4904-4047-9916-e585417a216f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68001-624-01 | 68001062401 | 1 BLISTER PACK in 1 CARTON (68001-624-01) / 21 TABLET in 1 BLISTER PACK | 1 blister pack | 2025-05-01 | Yes | No | Current |