Venlafaxine Hydrochloride
- Product NDC
- 70518-4154
- 11-digit product format
- 705184154
- Labeler code
- 70518
- Product ID
- 70518-4154_3d2fd9c4-1d5b-4f39-e063-6294a90a31ad
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VENLAFAXINE HYDROCHLORIDE
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA214654
- Marketing category
- ANDA
- Marketing start
- 2024-08-07
- 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 |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4154-0 | 70518415400 | 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-4154-0) | 2024-08-07 | No | No | Historical |
| 70518-4154-1 | 70518415401 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4154-1) | 2025-08-11 | No | No | Historical |
| 70518-4154-2 | 70518415402 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4154-2) | 2025-08-22 | No | No | Historical |