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NDC 57664-0508-13 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 Sun Pharmaceutical Industries, 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: 57664-0508-13
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Citalopram

Product Information

NDC	57664-0508
Product ID	57664-508_ef44872c-ba5e-d69b-e053-2a95a90adb55
Associated GPIs	58160020100320
GCN Sequence Number	046203
GCN Sequence Number Description	citalopram hydrobromide TABLET 20 MG ORAL
HIC3	H2S
HIC3 Description	SELECTIVE SEROTONIN REUPTAKE INHIBITOR (SSRIS)
GCN	16342
HICL Sequence Number	010321
HICL Sequence Number Description	CITALOPRAM HYDROBROMIDE
Brand/Generic	Generic
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	Sun Pharmaceutical Industries, Inc.
Pharmaceutical Class	Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA077032
Listing Certified Through	2024-12-31

Package

NDC 57664-0508-13 (57664050813)

Pricing Information	N/A
NDC Package Code	57664-508-13
Billing NDC	57664050813
Package	500 TABLET in 1 BOTTLE (57664-508-13)
Marketing Start Date	2015-05-29
NDC Exclude Flag	N