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Tamoxifen Citrate - 0093-0782-01 - (Tamoxifen Citrate)

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Drug Information of Tamoxifen Citrate

Product NDC: 0093-0782
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: 0093-0782
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074858
Marketing Category: ANDA
Start Marketing Date: 20030221

Package Information of Tamoxifen Citrate

Package NDC: 0093-0782-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0093-0782-01)

NDC Information of Tamoxifen Citrate

NDC Code 0093-0782-01
Proprietary Name Tamoxifen Citrate
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0093-0782-01)
Product NDC 0093-0782
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tamoxifen Citrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20030221
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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


General Information