MethylPREDNISolone
- Product NDC
- 63739-133
- 11-digit product format
- 637390133
- Labeler code
- 63739
- Product ID
- 63739-133_2d1b064c-c50f-4168-b66b-f956795d18e8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA040183
- Marketing category
- ANDA
- Marketing start
- 1998-12-22
- 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
FDA-Initiated Inactive NDC Indexing#