Venlafaxine Hydrochloride
- Product NDC
- 82804-038
- 11-digit product format
- 828040038
- Labeler code
- 82804
- Product ID
- 82804-038_5c558ab8-b4b3-4973-b016-ed5cfcb4d88b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA200834
- Marketing category
- ANDA
- Marketing start
- 2011-11-23
- 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 |
|---|
| 82804-038-30 | 82804003830 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82804-038-30) | 2023-11-07 | No | No | Historical |
| 82804-038-60 | 82804003860 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82804-038-60) | 2023-11-07 | No | No | Historical |
| 82804-038-90 | 82804003890 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82804-038-90) | 2023-11-07 | No | No | Historical |