Methylprednisolone
- Product NDC
- 70518-1541
- 11-digit product format
- 705181541
- Labeler code
- 70518
- Product ID
- 70518-1541_d9a1828b-0296-0a20-e053-2a95a90a4838
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040194
- Marketing category
- ANDA
- Marketing start
- 2018-10-16
- Marketing end
- 0000-00-00
- Substance
- METHYLPREDNISOLONE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70518-1541-0 | 70518154100 | 1 DOSE PACK in 1 CARTON (70518-1541-0) > 21 TABLET in 1 DOSE PACK | 1 dose pack | 2018-10-16 | 0000-00-00 | No | No | Current |