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"71335-2109-8" National Drug Code (NDC)

Doxycycline 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2109-8)
(Bryant Ranch Prepack)

NDC Code71335-2109-8
Package Description21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2109-8)
Product NDC71335-2109
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDoxycycline
Non-Proprietary NameDoxycycline
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20051208
Marketing Category NameANDA
Application NumberANDA065285
ManufacturerBryant Ranch Prepack
Substance NameDOXYCYCLINE
Strength100
Strength Unitmg/1
Pharmacy ClassesTetracycline-class Drug [EPC], Tetracyclines [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-2109-8





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