Supplier processes active pharmaceutical ingredient (API) with modern purification technologies and has reliable traceability to the starting material. USP testing is performed prior to shipping API.
After receiving API, APP conducts USP testing for quality and purity.
API is converted into injectable heparin; samples undergo chemistry and microbiology testing.
Multiple U.S. based manufacturing facilities with proven capacity
to supply 100% of the U.S.
heparin market.
Thorough inspection is conducted before packaging and labeling.
Label is bar coded, and features bolder, larger typefaces and notations.
Finished product is tested to ensure it meets USP standards.
Over the past 3 years, APP has supplied and distributed over 200 million vials of heparin.*
*APP data on file.
- APP API supplier
- APP receives API from supplier
- Heparin is formulated
- Heparin is filled into vials
- Every vial is inspected
- Product labeled and packaged
- Final check
- Heparin distributed
® and APP® are registered trademarks of APP Pharmaceuticals, LLC.