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Neuro-Pro T007

Active substance: .GAMMA.-AMINOBUTYRIC ACID, LEVODOPA, NOREPINEPHRINE, SEROTONIN HYDROCHLORIDE, CORTICOTROPIN, ANACARDIUM OCCIDENTALE FRUIT, ARSENIC TRIOXIDE, BARIUM CARBONATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, TRIBASIC CALCIUM PHOSPHATE, HYOSCYAMUS NIGER, LYCOPODIUM CLAVATUM SPORE, DATURA STRAMONIUM

LIQUID · .GAMMA.-AMINOBUTYRIC ACID 6 [hp_X]/mL, LEVODOPA 6 [hp_X]/mL, NOREPINEPHRINE 6 [hp_X]/mL, SEROTONIN HYDROCHLORIDE 6 [hp_X]/mL, CORTICOTROPIN 8 [hp_X]/mL, ANACARDIUM OCCIDENTALE FRUIT 30 [hp_C]/mL, ARSENIC TRIOXIDE 30 [hp_C]/mL, BARIUM CARBONATE 30 [hp_C]/mL, OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_C]/mL, TRIBASIC CALCIUM PHOSPHATE 30 [hp_C]/mL, HYOSCYAMUS NIGER 30 [hp_C]/mL, LYCOPODIUM CLAVATUM SPORE 30 [hp_C]/mL, DATURA STRAMONIUM 30 [hp_C]/mL

United StatesActive

Marketing holder: Guangzhou Renuma Medical Systems Co., Ltd

Verified 2026-10-09 · openFDA NDC

Analogues in other countries
Composition
Products containing levodopa in other countries

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

CountryProducts
RU 28
  • Бензиэль®
    таблетки, 200 мг+50 мг (original in Russian, GRLS)
    ЛП-№(004140)-(РГ-RU)
    Закрытое акционерное общество "Канонфарма продакшн" (ЗАО "Канонфарма продакшн")
  • Бензиэль®
    таблетки, 200 мг+50 мг (original in Russian, GRLS)
    ЛП-005725
    Закрытое акционерное общество "Канонфарма продакшн" (ЗАО "Канонфарма продакшн")
  • Дуодопа®
    гель для интестинального введения, 20 мг/мл+5 мг/мл, 100 мл (original in Russian, GRLS)
    ЛП-№(014575)-(РГ-RU)
    Общество с ограниченной ответственностью "ЭббВи"
  • Дуодопа®
    гель для интестинального введения, 20 мг/мл+5 мг/мл, 100 мл (original in Russian, GRLS)
    ЛП-003027
    Общество с ограниченной ответственностью "ЭббВи"
  • Леводопа
    субстанция-порошок, ~, 25 кг (original in Russian, GRLS)
    ФС-000939
    Гуанси Чжуан Нэшионэлити Аутономос Риджен Лин Юнь Фармасьютикал Фэктори
All products in this country (28)
EU 7All products in this country (7)
Registration
Registration number
71742-0001
Registration status
Active
Dispensing
Over the counter
Route
ORAL
Sources
  • product · openFDA NDC · 71742-0001 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 71742-0001 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 71742-0001 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 71742-0001 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 71742-0001 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 71742-0001 · Verified 2026-10-09 · open in source
  • ingredients.4 · openFDA NDC · 71742-0001 · Verified 2026-10-09 · open in source
  • ingredients.5 · openFDA NDC · 71742-0001 · Verified 2026-10-09 · open in source
  • ingredients.6 · openFDA NDC · 71742-0001 · Verified 2026-10-09 · open in source
  • ingredients.7 · openFDA NDC · 71742-0001 · Verified 2026-10-09 · open in source
  • ingredients.8 · openFDA NDC · 71742-0001 · Verified 2026-10-09 · open in source
  • ingredients.9 · openFDA NDC · 71742-0001 · Verified 2026-10-09 · open in source
  • ingredients.10 · openFDA NDC · 71742-0001 · Verified 2026-10-09 · open in source
  • ingredients.11 · openFDA NDC · 71742-0001 · Verified 2026-10-09 · open in source
  • ingredients.12 · openFDA NDC · 71742-0001 · Verified 2026-10-09 · open in source