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NDC 50771-0001-02 Venlafaxine Hydrochloride 25 mg/1 Details
Venlafaxine Hydrochloride 25 mg/1
Venlafaxine Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Yaopharma Co., Ltd.. The primary component is VENLAFAXINE HYDROCHLORIDE.
MedlinePlus Drug Summary
Venlafaxine is used to treat depression. Venlafaxine extended-release (long-acting) capsules are also used to treat generalized anxiety disorder (GAD; excessive worrying that is difficult to control), social anxiety disorder (extreme fear of interacting with others or performing in front of others that interferes with normal life), and panic disorder (sudden, unexpected attacks of extreme fear and worry about these attacks). Venlafaxine is in a class of medications called selective serotonin and norepinephrine reuptake inhibitors (SNRIs). It works by increasing the amounts of serotonin and norepinephrine, natural substances in the brain that help maintain mental balance.
Related Packages: 50771-0001-02Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Venlafaxine
Product Information
| NDC | 50771-0001 |
|---|---|
| Product ID | 50771-001_fc073e2e-4b2a-3a3d-e053-6294a90a5037 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Venlafaxine Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | venlafaxine hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 25 |
| Active Ingredient Units | mg/1 |
| Substance Name | VENLAFAXINE HYDROCHLORIDE |
| Labeler Name | Yaopharma Co., Ltd. |
| Pharmaceutical Class | Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA202036 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 50771-0001-02 (50771000102)
| NDC Package Code | 50771-001-02 |
|---|---|
| Billing NDC | 50771000102 |
| Package | 100 TABLET in 1 BOTTLE, PLASTIC (50771-001-02) |
| Marketing Start Date | 2016-09-06 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |