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NDC 70518-1040-00 Sertraline 100 mg/1 Details
Sertraline 100 mg/1
Sertraline is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is SERTRALINE HYDROCHLORIDE.
MedlinePlus Drug Summary
Sertraline is used to treat depression, obsessive-compulsive disorder (bothersome thoughts that won't go away and the need to perform certain actions over and over), panic attacks (sudden, unexpected attacks of extreme fear and worry about these attacks), posttraumatic stress disorder (disturbing psychological symptoms that develop after a frightening experience), and social anxiety disorder (extreme fear of interacting with others or performing in front of others that interferes with normal life). It is also used to relieve the symptoms of premenstrual dysphoric disorder, including mood swings, irritability, bloating, and breast tenderness. Sertraline is in a class of antidepressants called selective serotonin reuptake inhibitors (SSRIs). It works by increasing the amounts of serotonin, a natural substance in the brain that helps maintain mental balance.
Related Packages: 70518-1040-00Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Sertraline
Product Information
| NDC | 70518-1040 |
|---|---|
| Product ID | 70518-1040_f8af26fc-0ddc-2204-e053-6294a90a4a15 |
| 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 | Sertraline |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Sertraline |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 100 |
| Active Ingredient Units | mg/1 |
| Substance Name | SERTRALINE HYDROCHLORIDE |
| Labeler Name | REMEDYREPACK INC. |
| Pharmaceutical Class | Cytochrome P450 2D6 Inhibitors [MoA], Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA077670 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 70518-1040-00 (70518104000)
| NDC Package Code | 70518-1040-0 |
|---|---|
| Billing NDC | 70518104000 |
| Package | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1040-0) |
| Marketing Start Date | 2018-03-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |