Citalopram - 21695-030-00 - (Citalopram Hydrobromide)

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Drug Information of Citalopram

Product NDC: 21695-030
Proprietary Name: Citalopram
Non Proprietary Name: Citalopram Hydrobromide
Active Ingredient(s): 10    mg/1 & nbsp;   Citalopram Hydrobromide
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Citalopram

Product NDC: 21695-030
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078216
Marketing Category: ANDA
Start Marketing Date: 20070327

Package Information of Citalopram

Package NDC: 21695-030-00
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (21695-030-00)

NDC Information of Citalopram

NDC Code 21695-030-00
Proprietary Name Citalopram
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (21695-030-00)
Product NDC 21695-030
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram Hydrobromide
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070327
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
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


General Information