venlafaxine
- Product NDC
- 50090-4805
- 11-digit product format
- 500904805
- Labeler code
- 50090
- Product ID
- 50090-4805_71dde35d-89d6-40d9-bc2d-9e2c2b27db4d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078932
- Marketing category
- ANDA
- Marketing start
- 2015-10-01
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 38 mg/1
- Pharmacologic classes
- Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7D7RX5A8MO | VENLAFAXINE HYDROCHLORIDE | 99300-78-4 | VENLAFAXINE HYDROCHLORIDE |
| GRZ5RCB1QG | VENLAFAXINE | 93413-69-5 | venlafaxine |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4805-0 | 50090480500 | 30 TABLET in 1 BOTTLE (50090-4805-0) | 30 tablet | 2019-12-20 | 0000-00-00 | No | No | Current |
| 50090-4805-1 | 50090480501 | 90 TABLET in 1 BOTTLE (50090-4805-1) | 90 tablet | 2019-12-20 | 0000-00-00 | No | No | Current |