METHYLPREDNISOLONE
- Product NDC
- 71205-453
- 11-digit product format
- 712050453
- Labeler code
- 71205
- Product ID
- 71205-453_51700a49-0de1-4113-aee8-a57b380cd0d3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METHYLPREDNISOLONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA204072
- Marketing category
- ANDA
- Marketing start
- 2018-05-14
- 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 |
|---|
| 71205-453-21 | 71205045321 | 1 BLISTER PACK in 1 CARTON (71205-453-21) / 21 TABLET in 1 BLISTER PACK | 1 blister pack | 2020-05-20 | No | No | Historical |