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Meprobamate

Active substance: meprobamate

TABLET · MEPROBAMATE 200 mg/1

United StatesActive

Marketing holder: Alembic Pharmaceuticals Inc.

Verified 2026-10-09 · openFDA NDC

Composition
Import and control

Control by country

  • United StatescontrolledSchedule: CIV

    Source: openFDA NDC · record 01a1208d-9907-72d0-8d8d-fc3f2a52832d,01a12092-190e-7909-aaa8-dd07e9a1254c,01a12093-78f9-72e0-b3f7-f67935e43c55,01a12094-8b30-773f-bbb8-db08ccb860d8,01a12096-9e49-7d23-84cb-4d35585041db;count=6 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
62332-019
Registration status
Active
Dispensing
Prescription only
Control marker
CIV
Route
ORAL
Sources
  • product · openFDA NDC · 62332-019 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 62332-019 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 62332-019 · Verified 2026-10-09 · open in source