METHYLPREDNISOLONE
- Product NDC
- 50742-189
- 11-digit product format
- 507420189
- Labeler code
- 50742
- Product ID
- 50742-189_27eb4db1-87bf-4af7-a238-f24c0e43d5fb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA210985
- Marketing category
- ANDA
- Marketing start
- 2019-01-17
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50742-189-01 | 50742018901 | 100 TABLET in 1 BOTTLE (50742-189-01) | 100 tablet | 2019-01-17 | 0000-00-00 | No | No | Current |
| 50742-189-21 | 50742018921 | 1 BLISTER PACK in 1 CARTON (50742-189-21) > 21 TABLET in 1 BLISTER PACK | 1 blister pack | 2019-01-17 | 0000-00-00 | No | No | Current |