Desvenlafaxine Succinate
- Product NDC
- 59762-1211
- 11-digit product format
- 597621211
- Labeler code
- 59762
- Product ID
- 59762-1211_8b591edd-a797-4d94-9b0f-74e046df7e67
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- desvenlafaxine succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Greenstone LLC
- Application
- NDA021992
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2017-03-01
- Marketing end
- 0000-00-00
- Substance
- DESVENLAFAXINE SUCCINATE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Cytochrome P450 2D6 Inhibitors [MoA], Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [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 RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59762-1211-3 | 59762121103 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (59762-1211-3) | 2017-03-01 | 0000-00-00 | No | No | Current |