Venlafaxine Hydrochloride
- Product NDC
- 68071-3638
- 11-digit product format
- 680713638
- Labeler code
- 68071
- Product ID
- 68071-3638_1bf78ac7-07d7-dcb7-e063-6294a90aa6cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA214654
- Marketing category
- ANDA
- Marketing start
- 2022-09-07
- 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 |
|---|
| 68071-3638-3 | 68071363803 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-3638-3) | 2024-06-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Venlafaxine Hydrochloride | NuCare Pharmaceuticals,Inc. | 2024-06-28 | HUMAN PRESCRIPTION DRUG LABEL | 1 |