Methylprednisolone
- Product NDC
- 63187-802
- 11-digit product format
- 631870802
- Labeler code
- 63187
- Product ID
- 63187-802_5b5f70c9-c6e5-4f54-86e2-b659d3c7e616
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA040232
- Marketing category
- ANDA
- Marketing start
- 2016-05-26
- 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
- 2021-12-31
- 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 |
|---|
| 63187-802 | METHYLPREDNISOLONE TABLET [PROFICIENT RX LP] | 4 | Legacy NDC | 20200218_6cc22d98-754c-4f95-973f-c30055a10d2f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63187-802-21 | 63187080221 | 21 TABLET in 1 BLISTER PACK (63187-802-21) | 21 tablet | 2017-01-02 | 0000-00-00 | No | No | Current |