Venlafaxine Hydrochloride
- Product NDC
- 68820-106
- 11-digit product format
- 688200106
- Labeler code
- 68820
- Product ID
- 68820-106_4b03f280-f14e-4a58-9ebc-c32d56b2848c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Orchid Healthcare (a division of Orchid Chemicals & Pharmaceuticals Ltd.)
- Application
- ANDA091123
- Marketing category
- ANDA
- Marketing start
- 2012-07-07
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record