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NDC 65862-0006-10 Citalopram 20 mg/1 Details

Citalopram 20 mg/1

Citalopram is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Aurobindo Pharma Limited. 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: 65862-0006-10
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Citalopram

Product Information

NDC	65862-0006
Product ID	65862-006_6fc7097b-a847-4d83-a839-b41b566cf9ed
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
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	20
Active Ingredient Units	mg/1
Substance Name	CITALOPRAM HYDROBROMIDE
Labeler Name	Aurobindo Pharma Limited
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 65862-0006-10 (65862000610)

Pricing Information	N/A
NDC Package Code	65862-006-10
Billing NDC	65862000610
Package	10 BLISTER PACK in 1 CARTON (65862-006-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date	2004-10-28
NDC Exclude Flag	N