venlafaxine
- Product NDC
- 70934-941
- 11-digit product format
- 709340941
- Labeler code
- 70934
- Product ID
- 70934-941_d5e2bf56-c7fe-77a4-e053-2a95a90a004e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- venlafaxine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA078932
- Marketing category
- ANDA
- Marketing start
- 2022-01-12
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- 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
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 |
|---|
| 70934-941-30 | 70934094130 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-941-30) | 30 tablet | 2022-01-12 | 0000-00-00 | No | No | Current |