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NDC 68788-0802-03 Citalopram Hydrobromide 20 mg/1 Details

Citalopram Hydrobromide 20 mg/1

Citalopram Hydrobromide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred 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: 68788-0802-03
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Citalopram

Product Information

NDC	68788-0802
Product ID	68788-0802_d9295642-13dc-4089-83fb-d662003acafd
Associated GPIs	58160020100320
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 Hydrobromide
Proprietary Name Suffix	n/a
Non-Proprietary Name	Citalopram Hydrobromide
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	Preferred Pharmaceuticals, Inc.
Pharmaceutical Class	Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA078216
Listing Certified Through	2024-12-31

Package

NDC 68788-0802-03 (68788080203)

Pricing Information	N/A
NDC Package Code	68788-0802-3
Billing NDC	68788080203
Package	30 TABLET in 1 BOTTLE (68788-0802-3)
Marketing Start Date	2013-03-26
NDC Exclude Flag	N