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Tamoxifen Citrate - 0378-0144-91 - (Tamoxifen Citrate)

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Drug Information of Tamoxifen Citrate

Product NDC: 0378-0144
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: 0378-0144
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074732
Marketing Category: ANDA
Start Marketing Date: 20130509

Package Information of Tamoxifen Citrate

Package NDC: 0378-0144-91
Package Description: 60 TABLET in 1 BOTTLE (0378-0144-91)

NDC Information of Tamoxifen Citrate

NDC Code 0378-0144-91
Proprietary Name Tamoxifen Citrate
Package Description 60 TABLET in 1 BOTTLE (0378-0144-91)
Product NDC 0378-0144
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tamoxifen Citrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130509
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
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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