Desvenlafaxine
- Product NDC
- 51407-021
- 11-digit product format
- 514070021
- Labeler code
- 51407
- Product ID
- 51407-021_99883f62-8c2f-1907-e053-2995a90a0d10
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desvenlafaxine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA204065
- Marketing category
- ANDA
- Marketing start
- 2016-07-29
- Marketing end
- 0000-00-00
- Substance
- DESVENLAFAXINE SUCCINATE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record