Venlafaxine Hydrochloride
- Product NDC
- 50090-7317
- 11-digit product format
- 500907317
- Labeler code
- 50090
- Product ID
- 50090-7317_2b88c796-27c3-478e-b48b-85b47e5f90af
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VENLAFAXINE HYDROCHLORIDE
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA214654
- Marketing category
- ANDA
- Marketing start
- 2022-09-07
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 75 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 |
|---|
| 50090-7317-0 | 50090731700 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7317-0) | 2024-10-14 | No | No | Historical |
| 50090-7317-1 | 50090731701 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7317-1) | 2024-10-14 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Venlafaxine Hydrochloride | A-S Medication Solutions | 2024-10-16 | HUMAN PRESCRIPTION DRUG LABEL | 1 |