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"70069-848-30" National Drug Code (NDC)
Rilpivirine 30 TABLET, FILM COATED in 1 BOTTLE (70069-848-30)
(Somerset Therapeutics, LLC)
NDC Code
70069-848-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (70069-848-30)
Product NDC
70069-848
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Rilpivirine
Non-Proprietary Name
Rilpivirine
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20260130
Marketing Category Name
ANDA
Application Number
ANDA218798
Manufacturer
Somerset Therapeutics, LLC
Substance Name
RILPIVIRINE HYDROCHLORIDE
Strength
25
Strength Unit
mg/1
Pharmacy Classes
Human Immunodeficiency Virus 1 Non-Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Non-Nucleoside Analog [EXT], Non-Nucleoside Reverse Transcriptase Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70069-848-30