Methylprednisolone
- Product NDC
- 69306-004
- 11-digit product format
- 693060004
- Labeler code
- 69306
- Product ID
- 69306-004_eb848bd5-eb69-58b1-e053-2a95a90a577e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylprednisolone
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Doc Rx
- Application
- ANDA040189
- Marketing category
- ANDA
- Marketing start
- 1997-10-31
- 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 Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69306-004 | METHYLPREDNISOLONE TABLET [DOC RX] | 2 | Legacy NDC | 20221022_8e075a62-34a0-4118-bd85-78328a04fa2e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69306-004-21 | 69306000421 | 21 TABLET in 1 BLISTER PACK (69306-004-21) | 21 tablet | 2020-02-27 | 0000-00-00 | No | No | Current |