Methylprednisolone
- Product NDC
- 60760-373
- 11-digit product format
- 607600373
- Labeler code
- 60760
- Product ID
- 60760-373_92230b4a-8e6d-dbbf-e053-2995a90aadef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA040194
- Marketing category
- ANDA
- Marketing start
- 2019-09-05
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-373-21 | 60760037321 | 1 DOSE PACK in 1 CARTON (60760-373-21) > 21 TABLET in 1 DOSE PACK | 1 dose pack | 2019-09-05 | 0000-00-00 | No | No | Current |