Methylprednisolone
- Product NDC
- 71205-054
- 11-digit product format
- 712050054
- Labeler code
- 71205
- Product ID
- 71205-054_466725dd-44bf-4405-9ec6-f7a05a0b63f9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA040194
- Marketing category
- ANDA
- Marketing start
- 1997-10-31
- 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 |
|---|
| 71205-054 | METHYLPREDNISOLONE TABLET [PROFICIENT RX LP] | 4 | Legacy NDC | 20200229_e54a5e33-ddd2-4da0-9f67-12b71edd4af7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-054-21 | 71205005421 | 21 TABLET in 1 BOTTLE (71205-054-21) | 21 tablet | 2018-06-01 | 0000-00-00 | No | No | Current |