Venlafaxine
- Product NDC
- 70518-4500
- 11-digit product format
- 705184500
- Labeler code
- 70518
- Product ID
- 70518-4500_4109ea54-b204-364e-e063-6394a90a0b9a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA214127
- Marketing category
- ANDA
- Marketing start
- 2025-10-12
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 150 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4500-0 | 70518450000 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4500-0) | 2025-10-12 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Venlafaxine | REMEDYREPACK INC. | 2025-10-13 | HUMAN PRESCRIPTION DRUG LABEL | 1 |