Venlafaxine
- Product NDC
- 71335-9704
- 11-digit product format
- 713359704
- Labeler code
- 71335
- Product ID
- 71335-9704_1471508e-7fe4-43db-94ea-b4df1bcbafa9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077653
- Marketing category
- ANDA
- Marketing start
- 2008-06-13
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 37.5 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
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 71335-9704-1 | 71335970401 | 30 TABLET in 1 BOTTLE (71335-9704-1) | 30 tablet | 2023-04-24 | No | No | Historical |
| 71335-9704-2 | 71335970402 | 60 TABLET in 1 BOTTLE (71335-9704-2) | 60 tablet | 2023-06-27 | No | No | Historical |
| 71335-9704-3 | 71335970403 | 90 TABLET in 1 BOTTLE (71335-9704-3) | 90 tablet | 2023-10-10 | No | No | Historical |
| 71335-9704-4 | 71335970404 | 10 TABLET in 1 BOTTLE (71335-9704-4) | 10 tablet | 2024-04-05 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Venlafaxine Tablets, USP | Bryant Ranch Prepack | 2024-04-05 | HUMAN PRESCRIPTION DRUG LABEL | 101 |