Venlafaxine Hydrochloride
- Product NDC
- 0615-8509
- 11-digit product format
- 006158509
- Labeler code
- 0615
- Product ID
- 0615-8509_f4c48a47-b134-4ed0-a838-0af90d59dc5d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA217390
- Marketing category
- ANDA
- Marketing start
- 2023-09-25
- 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 |
|---|
| 0615-8509-39 | 00615850939 | 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0615-8509-39) | 2024-05-16 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Venlafaxine Hydrochloride | NCS HealthCare of KY, LLC dba Vangard Labs | 2024-06-19 | HUMAN PRESCRIPTION DRUG LABEL | 1 |