methylprednisolone
- Product NDC
- 68788-8276
- 11-digit product format
- 687888276
- Labeler code
- 68788
- Product ID
- 68788-8276_07be62fa-ccd2-4243-b588-3fb1ac17d66d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA206751
- Marketing category
- ANDA
- Marketing start
- 2022-10-14
- Marketing end
- 0000-00-00
- Substance
- METHYLPREDNISOLONE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-8276 | METHYLPREDNISOLONE TABLET [PREFERRED PHARMACEUTICALS INC.] | 3 | Legacy NDC | 20240716_07be62fa-ccd2-4243-b588-3fb1ac17d66d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8276-2 | 68788827602 | 1 BLISTER PACK in 1 CARTON (68788-8276-2) > 21 TABLET in 1 BLISTER PACK | 1 blister pack | 2022-10-14 | 0000-00-00 | No | No | Current |