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Tamoxifen Citrate - 54868-4287-2 - (Tamoxifen Citrate)

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Drug Information of Tamoxifen Citrate

Product NDC: 54868-4287
Proprietary Name: Tamoxifen Citrate
Non Proprietary Name: Tamoxifen Citrate
Active Ingredient(s): 20    mg/1 & nbsp;   Tamoxifen Citrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Tamoxifen Citrate

Product NDC: 54868-4287
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074858
Marketing Category: ANDA
Start Marketing Date: 20050117

Package Information of Tamoxifen Citrate

Package NDC: 54868-4287-2
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (54868-4287-2)

NDC Information of Tamoxifen Citrate

NDC Code 54868-4287-2
Proprietary Name Tamoxifen Citrate
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (54868-4287-2)
Product NDC 54868-4287
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tamoxifen Citrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050117
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name TAMOXIFEN CITRATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Estrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA]

Complete Information of Tamoxifen Citrate


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