Venlafaxine Hydrochloride
- Product NDC
- 80425-0290
- 11-digit product format
- 804250290
- Labeler code
- 80425
- Product ID
- 80425-0290_2a9bad62-b303-697c-e063-6294a90aa395
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Advanced Rx Pharmacy of Tennessee, LLC
- Application
- ANDA214654
- Marketing category
- ANDA
- Marketing start
- 2023-03-24
- 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 |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 80425-0290-1 | 80425029001 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (80425-0290-1) | 2023-03-24 | No | No | Historical |
| 80425-0290-2 | 80425029002 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (80425-0290-2) | 2023-03-24 | No | No | Historical |
| 80425-0290-3 | 80425029003 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (80425-0290-3) | 2023-03-24 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Venlafaxine HCL ER Tablets | Advanced Rx Pharmacy of Tennessee, LLC | 2024-12-31 | HUMAN PRESCRIPTION DRUG LABEL | 2 |