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"0093-0782-10" National Drug Code (NDC)

Tamoxifen Citrate 1000 TABLET, FILM COATED in 1 BOTTLE (0093-0782-10)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-0782-10
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (0093-0782-10)
Product NDC0093-0782
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTamoxifen Citrate
Non-Proprietary NameTamoxifen Citrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20030221
End Marketing Date20190228
Marketing Category NameANDA
Application NumberANDA074858
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameTAMOXIFEN CITRATE
Strength20
Strength Unitmg/1
Pharmacy ClassesEstrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-0782-10





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