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NDC 43063-0670-30 Citalopram 40 mg/1 Details
Citalopram 40 mg/1
Citalopram is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. 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: 43063-0670-30Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Citalopram
Product Information
NDC | 43063-0670 |
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Product ID | 43063-670_f692d818-1622-126c-e053-2995a90ad54d |
Associated GPIs | 58160020100340 |
GCN Sequence Number | 046204 |
GCN Sequence Number Description | citalopram hydrobromide TABLET 40 MG ORAL |
HIC3 | H2S |
HIC3 Description | SELECTIVE SEROTONIN REUPTAKE INHIBITOR (SSRIS) |
GCN | 16343 |
HICL Sequence Number | 010321 |
HICL Sequence Number Description | CITALOPRAM HYDROBROMIDE |
Brand/Generic | Generic |
Proprietary Name | Citalopram |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Citalopram Hydrobromide |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET, FILM COATED |
Route | ORAL |
Active Ingredient Strength | 40 |
Active Ingredient Units | mg/1 |
Substance Name | CITALOPRAM HYDROBROMIDE |
Labeler Name | PD-Rx Pharmaceuticals, Inc. |
Pharmaceutical Class | Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA077031 |
Listing Certified Through | 2024-12-31 |
Package
NDC 43063-0670-30 (43063067030)
NDC Package Code | 43063-670-30 |
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Billing NDC | 43063067030 |
Package | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-670-30) |
Marketing Start Date | 2016-04-29 |
NDC Exclude Flag | N |
Pricing Information | N/A |