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NDC 72789-0071-30 Citalopram Hydrobromide 40 mg/1 Details

Citalopram Hydrobromide 40 mg/1

Citalopram Hydrobromide is a ORAL TABLET 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: 72789-0071-30
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Citalopram

Product Information

NDC	72789-0071
Product ID	72789-071_030efd44-9b54-b8d4-e063-6394a90a1340
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 Hydrobromide
Proprietary Name Suffix	n/a
Non-Proprietary Name	Citalopram Hydrobromide
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
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	ANDA078216
Listing Certified Through	2024-12-31

Package

NDC 72789-0071-30 (72789007130)

Pricing Information	N/A
NDC Package Code	72789-071-30
Billing NDC	72789007130
Package	30 TABLET in 1 BOTTLE, PLASTIC (72789-071-30)
Marketing Start Date	2020-05-15
NDC Exclude Flag	N