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"51862-642-10" National Drug Code (NDC)

Tamoxifen Citrate 1000 TABLET, FILM COATED in 1 BOTTLE (51862-642-10)
(Mayne Pharma Commercial LLC)

NDC Code51862-642-10
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (51862-642-10)
Product NDC51862-642
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTamoxifen Citrate
Non-Proprietary NameTamoxifen Citrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210827
Marketing Category NameANDA
Application NumberANDA075797
ManufacturerMayne Pharma Commercial LLC
Substance NameTAMOXIFEN CITRATE
Strength10
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/51862-642-10





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