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"71921-250-96" National Drug Code (NDC)

Lofexidine 1 BOTTLE in 1 CARTON (71921-250-96) / 96 TABLET, COATED in 1 BOTTLE
(Florida Pharmaceutical Products, LLC)

NDC Code71921-250-96
Package Description1 BOTTLE in 1 CARTON (71921-250-96) / 96 TABLET, COATED in 1 BOTTLE
Product NDC71921-250
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLofexidine
Non-Proprietary NameLofexidine
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20240821
Marketing Category NameANDA
Application NumberANDA218613
ManufacturerFlorida Pharmaceutical Products, LLC
Substance NameLOFEXIDINE HYDROCHLORIDE
Strength.18
Strength Unitmg/1

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71921-250-96





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