MethylPREDNISolone
- Product NDC
- 63629-2226
- 11-digit product format
- 636292226
- Labeler code
- 63629
- Product ID
- 63629-2226_02af0e7c-422a-fd56-e063-6394a90a9659
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040183
- Marketing category
- ANDA
- Marketing start
- 1998-12-22
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| X4W7ZR7023 | METHYLPREDNISOLONE | 83-43-2 | METHYLPREDNISOLONE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63629-2226-1 | 63629222601 | 1 DOSE PACK in 1 CARTON (63629-2226-1) / 21 TABLET in 1 DOSE PACK | 1 dose pack | 1998-12-22 | No | No | Historical |