Citalopram - 76237-136-30 - (Citalopram)

Alphabetical Index


Drug Information of Citalopram

Product NDC: 76237-136
Proprietary Name: Citalopram
Non Proprietary Name: Citalopram
Active Ingredient(s): 20    mg/1 & nbsp;   Citalopram
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Citalopram

Product NDC: 76237-136
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077048
Marketing Category: ANDA
Start Marketing Date: 20110901

Package Information of Citalopram

Package NDC: 76237-136-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-136-30) > 5 TABLET in 1 BLISTER PACK

NDC Information of Citalopram

NDC Code 76237-136-30
Proprietary Name Citalopram
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-136-30) > 5 TABLET in 1 BLISTER PACK
Product NDC 76237-136
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Citalopram
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110901
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
Substance Name CITALOPRAM HYDROBROMIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Citalopram


General Information