METHYLPREDNISOLONE
- Product NDC
- 60760-961
- 11-digit product format
- 607600961
- Labeler code
- 60760
- Product ID
- 60760-961_235cb8f6-e9c0-a547-e063-6394a90af553
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METHYLPREDNISOLONE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- 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 |
|---|
| 60760-961-21 | 60760096121 | 1 BLISTER PACK in 1 CARTON (60760-961-21) / 21 TABLET in 1 BLISTER PACK | 1 blister pack | 2024-09-06 | No | No | Historical |