Methylprednisolone
- Product NDC
- 0591-0790
- 11-digit product format
- 005910790
- Labeler code
- 0591
- Product ID
- 0591-0790_042a4f34-c640-483d-b255-0b8f9918fc72
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA040232
- Marketing category
- ANDA
- Marketing start
- 2016-05-26
- Marketing end
- 2021-09-30
- Substance
- METHYLPREDNISOLONE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 0591-0790-21 | 00591079021 | 21 TABLET in 1 BLISTER PACK (0591-0790-21) | 21 tablet | 2016-05-26 | 2021-09-30 | No | No | Current |