Methylprednisolone Sodium Succinate
- Product NDC
- 71329-302
- 11-digit product format
- 713290302
- Labeler code
- 71329
- Product ID
- 71329-302_5c22bf7e-4275-40f4-8502-fd9d34801557
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Methylprednisolone
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- GeneYork Pharmaceuticals Group LLC
- Application
- ANDA212396
- Marketing category
- ANDA
- Marketing start
- 2021-04-20
- Marketing end
- 0000-00-00
- Substance
- METHYLPREDNISOLONE SODIUM SUCCINATE
- Active strength
- 125 mg/2mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71329-302 | METHYLPREDNISOLONE SODIUM SUCCINATE (METHYLPREDNISOLONE) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [GENEYORK PHARMACEUTICALS GROUP LLC] | 3 | Legacy NDC | 20210428_23b17612-b122-4c89-80a7-5f3ca57fad7f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71329-302-25 | 71329030225 | 25 VIAL in 1 CARTON (71329-302-25) > 2 mL in 1 VIAL (71329-302-01) | 25 vial | 2021-04-20 | 0000-00-00 | No | No | Current |