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EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE

Active substance: EMTRICITABINE, TENOFOVIR DISOPROXIL FUMARATE

TABLET, FILM COATED · EMTRICITABINE 200 mg/1, TENOFOVIR DISOPROXIL FUMARATE 300 mg/1

United StatesActive

Marketing holder: DirectRx

Verified 2026-10-09 · openFDA NDC

Analogues in other countries
Composition
Products containing emtricitabine in other countries

Showing products with this active substance, combinations included; the full composition is shown for each product.

CountryProducts
RU 42
  • Биктарви®
    таблетки, покрытые пленочной оболочкой, 50 мг+25 мг+200 мг (original in Russian, GRLS)
    ЛП-№(006098)-(РГ-RU)
    Гилеад Сайенсиз Интернешнл Лтд.
  • Биктарви®
    таблетки, покрытые пленочной оболочкой, 50 мг+25 мг+200 мг (original in Russian, GRLS)
    ЛП-006054
    Гилеад Сайенсиз Интернешнл Лимитед
  • Генвоя®
    таблетки, покрытые пленочной оболочкой, 150 мг+10 мг+150 мг+200 мг (original in Russian, GRLS)
    ЛП-№(005222)-(РГ-RU)
    Гилеад Сайенсиз Интернешнл Лимитед
  • Генвоя®
    таблетки, покрытые пленочной оболочкой, 150 мг+10 мг+150 мг+200 мг (original in Russian, GRLS)
    ЛП-005722
    Гилеад Сайенсиз Интернешнл Лимитед
  • Доквир
    таблетки, покрытые пленочной оболочкой, 300 мг+200 мг (original in Russian, GRLS)
    ЛП-№(001732)-(РГ-RU)
    Акционерное общество "Фармасинтез" (АО "Фармасинтез")
All products in this country (42)
EU 19All products in this country (19)
Import and control

Control by country

  • Russiaprescription only

    Source: GRLS (Russian state register) · record 01a120c3-391f-7c93-9bdd-0023c50ab2b9,01a120c3-4132-7e5c-8fd8-bbb023758e32,01a120c3-77d7-74bc-a372-359293232bf8,01a120c4-b6a7-7d72-b9fe-7e0835d9e490,01a120c5-afdb-7677-9bd1-82b82d2bb560;count=7 · valid from 2026-10-09 · verified 2026-10-09

  • United Statesprescription only

    Source: openFDA NDC · record 01a12090-8a65-7bc2-bf24-bc2b9d105c9b,01a12095-677b-73c2-b1d9-d6c6d9234a15,01a12099-5176-7502-aae8-1f6f74595746,01a1209b-76a9-7efb-aadd-4717facd92f1,01a1209b-76af-781a-99b0-508910a2d231;count=5 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
72189-312
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 72189-312 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 72189-312 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 72189-312 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 72189-312 · Verified 2026-10-09 · open in source