Desvenlafaxine
- Product NDC
- 71335-0798
- 11-digit product format
- 713350798
- Labeler code
- 71335
- Product ID
- 71335-0798_e313351a-aab3-4e2b-bd2d-b378a4a6b36e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- desvenlafaxine
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204095
- Marketing category
- ANDA
- Marketing start
- 2017-03-01
- Marketing end
- 0000-00-00
- Substance
- DESVENLAFAXINE SUCCINATE
- Active strength
- 50 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record