Medrol
- Product NDC
- 70518-2041
- 11-digit product format
- 705182041
- Labeler code
- 70518
- Product ID
- 70518-2041_970fa816-6e05-b4e6-e053-2995a90a78d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA011153
- Marketing category
- NDA
- Marketing start
- 2019-04-26
- Marketing end
- 0000-00-00
- Substance
- METHYLPREDNISOLONE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record