Methylprednisolone
- Product NDC
- 62135-760
- 11-digit product format
- 621350760
- Labeler code
- 62135
- Product ID
- 62135-760_225669c1-9479-52eb-e063-6394a90a649b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA209097
- Marketing category
- ANDA
- Marketing start
- 2019-02-22
- 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 |
|---|
| 62135-760-01 | 62135076001 | 100 TABLET in 1 BOTTLE (62135-760-01) | 100 tablet | 2024-05-14 | No | No | Historical |
| 62135-760-21 | 62135076021 | 21 TABLET in 1 BOTTLE (62135-760-21) | 21 tablet | 2024-05-14 | No | No | Historical |