Overview

PHARMA-WALDHOF GMBH is an active pharmaceutical ingredient (API) supplier with 1 active FDA Type II Drug Master File, covering ADENOSINE.

API / Drug Master Files

PHARMA-WALDHOF GMBH holds 1 active (11 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.

  • ADENOSINEActive1988-10-25
  • URIDINE-5'-TRIPHOSPHATE (UTP), THERAPEUTIC GRADEInactive1996-09-20
  • N6-(2-ISOPENTENYL)-ADENOSINEInactive1990-08-17
  • 5-FLUORO-URACIL,PRODUCT 4965Inactive1983-05-18
  • ADENOSINE-5-MONOPHOSPHORIC ACID, PRODUCT #2030Inactive1982-05-04
  • URIDINE PRODUCT #3401Inactive1982-04-23
  • 5-BROMO-2' -DEOXYURIDINE (BDU)-PRODUCT NO. 6706Inactive1980-02-28
  • ADENINE AND ADENINE HCL (SYNTHETIC & FROM RNA OR ADENOSINE)Inactive1978-12-20
  • THYMIDINEInactive1978-06-20
  • GLUTATHIONE REDUCED (GSH)Inactive1977-11-09
  • GLUTATHIONE, OXIDIZED HYDRATEInactive1975-11-13

FDA compliance signals

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

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