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Citalopram Hydrobromide - 49349-414-02 - (Citalopram Hydrobromide)

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Drug Information of Citalopram Hydrobromide

Product NDC: 49349-414
Proprietary Name: Citalopram Hydrobromide
Non Proprietary Name: Citalopram Hydrobromide
Active Ingredient(s): 10    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: 49349-414
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077031
Marketing Category: ANDA
Start Marketing Date: 20110722

Package Information of Citalopram Hydrobromide

Package NDC: 49349-414-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-414-02)

NDC Information of Citalopram Hydrobromide

NDC Code 49349-414-02
Proprietary Name Citalopram Hydrobromide
Package Description 30 TABLET in 1 BLISTER PACK (49349-414-02)
Product NDC 49349-414
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram Hydrobromide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110722
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name CITALOPRAM HYDROBROMIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Citalopram Hydrobromide


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