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NDC 51655-0137-26 Citalopram 20 mg/1 Details
Citalopram 20 mg/1
Citalopram is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals, LLC. The primary component is CITALOPRAM HYDROBROMIDE.
MedlinePlus Drug Summary
Citalopram is used to treat depression. Citalopram is in a class of antidepressants called selective serotonin reuptake inhibitors (SSRIs). It works by increasing the amount of serotonin, a natural substance in the brain that helps maintain mental balance.
Related Packages: 51655-0137-26Last Updated: 04/21/2024
MedLinePlus Full Drug Details: Citalopram
Product Information
| NDC | 51655-0137 |
|---|---|
| Product ID | 51655-137_f2b42895-ae23-2d2b-e053-2995a90a899a |
| 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 | Citalopram |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Citalopram |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 20 |
| Active Ingredient Units | mg/1 |
| Substance Name | CITALOPRAM HYDROBROMIDE |
| Labeler Name | Northwind Pharmaceuticals, LLC |
| Pharmaceutical Class | Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA077534 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 51655-0137-26 (51655013726)
| NDC Package Code | 51655-137-26 |
|---|---|
| Billing NDC | 51655013726 |
| Package | 90 TABLET in 1 BOTTLE, PLASTIC (51655-137-26) |
| Marketing Start Date | 2023-01-19 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |