Methylprednisolone
- Product NDC
- 70518-2982
- 11-digit product format
- 705182982
- Labeler code
- 70518
- Product ID
- 70518-2982_eb0035ad-9fc7-6514-e053-2a95a90a9903
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040189
- Marketing category
- ANDA
- Marketing start
- 2021-01-07
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2982 | METHYLPREDNISOLONE TABLET [REMEDYREPACK INC.] | 5 | Legacy NDC | 20250409_94bf4bc7-0af8-400e-94da-a0f3440b5421.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2982-0 | 70518298200 | 21 TABLET in 1 BLISTER PACK (70518-2982-0) | 21 tablet | 2021-01-07 | 0000-00-00 | No | No | Current |