Venlafaxine
- Product NDC
- 60760-728
- 11-digit product format
- 607600728
- Labeler code
- 60760
- Product ID
- 60760-728_fab61465-dff5-0498-e053-6294a90a9aec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA077653
- Marketing category
- ANDA
- Marketing start
- 2023-04-21
- 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 |
|---|
| 60760-728-60 | 60760072860 | 60 TABLET in 1 BOTTLE, PLASTIC (60760-728-60) | 60 tablet | 2023-04-21 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Venlafaxine Tablets, USP | ST. MARY'S MEDICAL PARK PHARMACY | 2023-05-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |