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Tamoxifen Citrate - 60505-3035-7 - (Tamoxifen Citrate)

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Drug Information of Tamoxifen Citrate

Product NDC: 60505-3035
Proprietary Name: Tamoxifen Citrate
Non Proprietary Name: Tamoxifen Citrate
Active Ingredient(s): 10    mg/1 & nbsp;   Tamoxifen Citrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Tamoxifen Citrate

Product NDC: 60505-3035
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090878
Marketing Category: ANDA
Start Marketing Date: 20121130

Package Information of Tamoxifen Citrate

Package NDC: 60505-3035-7
Package Description: 180 TABLET in 1 BOTTLE (60505-3035-7)

NDC Information of Tamoxifen Citrate

NDC Code 60505-3035-7
Proprietary Name Tamoxifen Citrate
Package Description 180 TABLET in 1 BOTTLE (60505-3035-7)
Product NDC 60505-3035
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tamoxifen Citrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121130
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name TAMOXIFEN CITRATE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Estrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA]

Complete Information of Tamoxifen Citrate


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