METHYLPREDNISOLONE
- Product NDC
- 70625-237
- 11-digit product format
- 706250237
- Labeler code
- 70625
- Product ID
- 70625-237_e6eabd52-7f28-7adf-e053-2995a90af33c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Praxgen Pharmaceuticals LLC
- Application
- ANDA212262
- Marketing category
- ANDA
- Marketing start
- 2019-06-28
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70625-237-01 | 70625023701 | 100 TABLET in 1 BOTTLE (70625-237-01) | 100 tablet | 2019-06-28 | 0000-00-00 | No | No | Current |
| 70625-237-11 | 70625023711 | 1 DOSE PACK in 1 CARTON (70625-237-11) > 21 TABLET in 1 DOSE PACK | 1 dose pack | 2019-06-28 | 0000-00-00 | No | No | Current |