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NDC 70710-1698-00 Venlafaxine Hydrochloride 37.5 mg/1 Details
Venlafaxine Hydrochloride 37.5 mg/1
Venlafaxine Hydrochloride is a ORAL CAPSULE, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. 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: 70710-1698-00Last Updated: 05/12/2024
MedLinePlus Full Drug Details: Venlafaxine
Product Information
| NDC | 70710-1698 |
|---|---|
| Product ID | 70710-1698_29d6f5cb-58d4-4d82-966d-acd92b0431ee |
| 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 | CAPSULE, EXTENDED RELEASE |
| Route | ORAL |
| Active Ingredient Strength | 37.5 |
| Active Ingredient Units | mg/1 |
| Substance Name | VENLAFAXINE HYDROCHLORIDE |
| Labeler Name | Zydus Pharmaceuticals USA Inc. |
| 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 | ANDA090174 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70710-1698-00 (70710169800)
| NDC Package Code | 70710-1698-0 |
|---|---|
| Billing NDC | 70710169800 |
| Package | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1698-0) |
| Marketing Start Date | 2023-05-18 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |