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"70954-909-10" National Drug Code (NDC)

Lofexidine 36 TABLET in 1 BOTTLE (70954-909-10)
(ANI Pharmaceuticals, Inc.)

NDC Code70954-909-10
Package Description36 TABLET in 1 BOTTLE (70954-909-10)
Product NDC70954-909
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLofexidine
Non-Proprietary NameLofexidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20251022
Marketing Category NameANDA
Application NumberANDA219917
ManufacturerANI Pharmaceuticals, Inc.
Substance NameLOFEXIDINE HYDROCHLORIDE
Strength.18
Strength Unitmg/1

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