JENKEM TECHNOLOGY CO LTD
Overview
JENKEM TECHNOLOGY CO LTD is an active pharmaceutical ingredient (API) supplier with 14 active FDA Type II Drug Master Files, covering 4ARM PEG BROMOACETAMIDE (PENTAERYTHRITOL), HIGH PURITY MW 10000; 4ARM PEG SUCCINIMIDYL ADIPATE (PENTAERYTHRITOL) MW 20000; 4ARM PEG SUCCINIMIDYL GLUTARAMIDE (PENTAERYTHRITOL) MW 20000; 4ARM PEG SUCCINIMIDYL SUCCINATE (PENTAERYTHRITOL) MW 10000; 8ARM PEG SUCCINIMIDYL GLUTARATE (HEXAGLYCEROL) MW 15000; BIS-MONO-METHOXY BRANCHED POLYETHYLENE GLYCOL, N-HYDROXYSUCCINIMIDE ESTER (40KDA), OR MPEG2-NHS ESTER, 40KDA.
API / Drug Master Files
JENKEM TECHNOLOGY CO LTD holds 14 active (14 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.
- METHOXY PEG SUCCINIMIDYL CARBONATE, MW10000 (M-SC-10K)Active2026-01-30
- TBUO-ICO-GLU(AEEA-AEEA-OH)-OTBU (TIRZEPATIDE SIDE CHAIN)Active2024-12-12
- BIS-MONO-METHOXY BRANCHED POLYETHYLENE GLYCOL, N-HYDROXYSUCCINIMIDE ESTER (40KDA), OR MPEG2-NHS ESTER, 40KDAActive2023-08-09
- METHOXY PEG DITETRADECYLACETAMIDE (MW 2000), OR M-DTDAM-2000 (ALC-0159)Active2023-07-12
- MALEIMIDE-PEG2-SUCCINIMIDYL PROPIONATE, MW 425.4Active2022-09-28
- Y-SHAPE (MPEG20K)2-PEG10K MALEIMIDE, MW 50000Active2021-12-16
- METHOXY PEG PROPIONALDEHYDE MW 20000Active2021-09-23
- 4ARM PEG BROMOACETAMIDE (PENTAERYTHRITOL), HIGH PURITY MW 10000Active2020-04-20
- 4ARM PEG SUCCINIMIDYL GLUTARAMIDE (PENTAERYTHRITOL) MW 20000Active2019-07-23
- 4ARM PEG SUCCINIMIDYL ADIPATE (PENTAERYTHRITOL) MW 20000Active2019-07-23
- 4ARM PEG SUCCINIMIDYL SUCCINATE (PENTAERYTHRITOL) MW 10000Active2016-03-07
- METHOXY PEG SUCCINIMIDYL SUCCINATE MW20000Active2015-12-22
- 8ARM PEG SUCCINIMIDYL GLUTARATE (HEXAGLYCEROL) MW 15000Active2015-10-28
- Y-SHAPE PEG NHS ESTER, MW 40000 (NON-STERILE BULK FORM)Active2008-05-26
FDA compliance signals
No FDA recalls, Warning Letters, or Form 483 observations are linked to JENKEM TECHNOLOGY CO LTD in our records. PharmaTek screens the full directory against live FDA enforcement data.
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