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"0093-0782-01" National Drug Code (NDC)
Tamoxifen Citrate 100 TABLET, FILM COATED in 1 BOTTLE (0093-0782-01)
(Teva Pharmaceuticals USA, Inc.)
NDC Code
0093-0782-01
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (0093-0782-01)
Product NDC
0093-0782
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Tamoxifen Citrate
Non-Proprietary Name
Tamoxifen Citrate
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20030221
End Marketing Date
20190228
Marketing Category Name
ANDA
Application Number
ANDA074858
Manufacturer
Teva Pharmaceuticals USA, Inc.
Substance Name
TAMOXIFEN CITRATE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Estrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-0782-01