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citalopram hydrobromide - 43063-221-90 - (citalopram hydrobromide)

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Drug Information of citalopram hydrobromide

Product NDC: 43063-221
Proprietary Name: citalopram hydrobromide
Non Proprietary Name: citalopram hydrobromide
Active Ingredient(s): 40    mg/1 & nbsp;   citalopram hydrobromide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of citalopram hydrobromide

Product NDC: 43063-221
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077032
Marketing Category: ANDA
Start Marketing Date: 20041112

Package Information of citalopram hydrobromide

Package NDC: 43063-221-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (43063-221-90)

NDC Information of citalopram hydrobromide

NDC Code 43063-221-90
Proprietary Name citalopram hydrobromide
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (43063-221-90)
Product NDC 43063-221
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name citalopram hydrobromide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20041112
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name CITALOPRAM HYDROBROMIDE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of citalopram hydrobromide


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