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Citalopram Hydrobromide - 67046-116-30 - (Citalopram Hydrobromide)

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Drug Information of Citalopram Hydrobromide

Product NDC: 67046-116
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: 67046-116
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077044
Marketing Category: ANDA
Start Marketing Date: 20090901

Package Information of Citalopram Hydrobromide

Package NDC: 67046-116-30
Package Description: 30 TABLET in 1 BLISTER PACK (67046-116-30)

NDC Information of Citalopram Hydrobromide

NDC Code 67046-116-30
Proprietary Name Citalopram Hydrobromide
Package Description 30 TABLET in 1 BLISTER PACK (67046-116-30)
Product NDC 67046-116
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram Hydrobromide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090901
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
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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