Overview

EMBIO LTD is an active pharmaceutical ingredient (API) supplier with 4 active FDA Type II Drug Master Files, covering CANNABIDIOL-SYNTHETIC; EPHEDRINE SULFATE USP; PSEUDOEPHEDRINE HYDROCHLORIDE, USP; PSEUDOEPHEDRINE SULFATE USP.

API / Drug Master Files

EMBIO LTD holds 4 active (6 total) FDA Type II Drug Master Files — identifying it as an active-substance / API supplier. Type II DMFs are filed with the FDA to support the use of an active pharmaceutical ingredient in drug applications.

  • CANNABIDIOL-SYNTHETICActive2023-05-11
  • PSEUDOEPHEDRINE SULFATE USPActive2021-05-23
  • EPHEDRINE SULFATE USPActive2018-04-17
  • PSEUDOEPHEDRINE HYDROCHLORIDE, USPActive1998-12-29
  • PSEUDOEPHEDRINE SULFATE USPInactive2000-01-31
  • EPHEDRINE HYDROCHLORIDE USPInactive1991-08-09

FDA compliance signals

No FDA recalls, Warning Letters, or Form 483 observations are linked to EMBIO LTD in our records. PharmaTek screens the full directory against live FDA enforcement data.

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