Venlafaxine Hydrochloride
- Product NDC
- 53002-2366
- 11-digit product format
- 530022366
- Labeler code
- 53002
- Product ID
- 53002-2366_0c851fea-3353-4832-b5a1-931a502ccce2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA200834
- Marketing category
- ANDA
- Marketing start
- 2011-06-01
- Marketing end
- 0000-00-00
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 38 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-2366-3 | 53002236603 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (53002-2366-3) | 2021-01-01 | 0000-00-00 | No | No | Current |
| 53002-2366-9 | 53002236609 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (53002-2366-9) | 2021-01-01 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Venlafaxine Hydrochloride | RPK Pharmaceuticals, Inc. | 2022-03-30 | Human Prescription Drug Label | 1 |