METHYLPREDNISOLONE
- Product NDC
- 72647-331
- 11-digit product format
- 726470331
- Labeler code
- 72647
- Product ID
- 72647-331_95478ba5-65bc-4f31-b596-6417bed6f66c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- OAKRUM PHARMA, LLC
- Application
- ANDA212262
- Marketing category
- ANDA
- Marketing start
- 2019-11-12
- Marketing end
- 2024-01-31
- Substance
- METHYLPREDNISOLONE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 72647-331-01 | 72647033101 | 100 TABLET in 1 BOTTLE (72647-331-01) | 100 tablet | 2019-11-12 | 0000-00-00 | No | No | Current |
| 72647-331-04 | 72647033104 | 1 DOSE PACK in 1 CARTON (72647-331-04) > 21 TABLET in 1 DOSE PACK | 1 dose pack | 2019-11-12 | 0000-00-00 | No | No | Current |