Venlafaxine Hydrochloride
- Product NDC
- 71205-812
- 11-digit product format
- 712050812
- Labeler code
- 71205
- Product ID
- 71205-812_922388b3-fc1c-46c6-b314-9049bd042df7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA212277
- Marketing category
- ANDA
- Marketing start
- 2019-07-08
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Active strength
- 37.5 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 |
|---|
| 71205-812-30 | 71205081230 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-812-30) | 2023-06-02 | No | No | Historical |
| 71205-812-60 | 71205081260 | 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-812-60) | 2023-06-02 | No | No | Historical |
| 71205-812-90 | 71205081290 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71205-812-90) | 2023-06-02 | No | No | Historical |