"70069-848-30" National Drug Code (NDC)

Rilpivirine 30 TABLET, FILM COATED in 1 BOTTLE (70069-848-30)
(Somerset Therapeutics, LLC)

NDC Code70069-848-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (70069-848-30)
Product NDC70069-848
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRilpivirine
Non-Proprietary NameRilpivirine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20260130
Marketing Category NameANDA
Application NumberANDA218798
ManufacturerSomerset Therapeutics, LLC
Substance NameRILPIVIRINE HYDROCHLORIDE
Strength25
Strength Unitmg/1
Pharmacy ClassesHuman Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Non-Nucleoside Analog [EXT], Non-Nucleoside Reverse Transcriptase Inhibitors [MoA]

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