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LONG GROVE PHARMACEUTICALS
Icon Reference Guide
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LONG GROVE PHARMACEUTICALS
Icon Reference Guide
Where our products are made
![Made in the USA Made in the USA](https://longgrovepharma.com/wp-content/uploads/2024/02/MADEin-USA.png)
We are proud to utilize domestic manufacturing facilities to provide the highest quality generics to the U.S. pharmaceutical market. With a simplified supply chain and protection from international disruptions, we offer certainty and efficiency to our customers.
![Carboprost is made in Canada Carboprost is made in Canada](https://longgrovepharma.com/wp-content/uploads/2022/08/made-in-canada.png)
Utilizing Canadian facilities allows us to provide the highest quality generics while simultaneously helping to control costs. With a dedicated pipeline just across the border, we can increase certainty to our customers.
![Made in the EU Made in the EU](https://longgrovepharma.com/wp-content/uploads/2022/06/made-in-the-eu.png)
We are proud to partner with manufacturers in the European Union to provide new, incremental supply to the U.S. pharmaceutical market. These partnerships provide high quality generics and increased certainty to customers through dedicated supply chains.
Product Highlights
![TAA Compliant TAA Compliant](https://longgrovepharma.com/wp-content/uploads/2022/06/taa-compliant.png)
The Trade Agreements Act (TAA) was enacted to foster fair and open international trade and requires that government officials only procure goods manufactured in the U.S. or an approved designated country. Products are considered TAA compliant if they are manufactured or substantially transformed in the United States or any of the TAA designated countries. Having dedicated supply from established manufacturers in TAA compliant countries is another way Long Grove Pharmaceuticals addresses supply chain continuity.
![Carboprost vial presentation icon Carboprost vial presentation icon](https://longgrovepharma.com/wp-content/uploads/2022/08/vial-presentation.png)
We utilize vials as a preferred container for injectable products whenever possible to align with provider preference.
![Vial Stopper Not Made With Natural Rubber Latex Vial Stopper Not Made With Natural Rubber Latex](https://longgrovepharma.com/wp-content/uploads/2022/06/vial-stopper-not-made-with-rubber-latex.png)
When identified, Long Grove Pharmaceuticals’ vial stoppers are not made with natural rubber latex.
![preservative free preservative free](https://longgrovepharma.com/wp-content/uploads/2024/02/Asset-9pre-free.png)
When identified, Long Grove Pharmaceuticals’ products are formulated 100% preservative-free to ensure their safety and appropriateness for patients who cannot be administered preservatives.
![FDA APPROVED FDA APPROVED](https://longgrovepharma.com/wp-content/uploads/2024/02/FDA-APPROVED.png)
This product formulation has undergone rigorous FDA review and approval for prescription use.
![READT TO USE PREMIX READT TO USE PREMIX](https://longgrovepharma.com/wp-content/uploads/2024/02/RTU-PREMIX.png)
This product is designed with a ready-to-use premixed formulation that can improve patient safety and help enhance the efficiency of pharmacy operations by reducing the steps required to prepare the product for patient use.
![PVC FREE PVC FREE](https://longgrovepharma.com/wp-content/uploads/2024/02/PVC-FREE.png)
When identified, Long Grove Pharmaceuticals’ IV bags or primary containers are free of PVC and DEHP.
Therapeutic Equivalency Rating
![Therapeutic Equivalency AB Rated Therapeutic Equivalency AB Rated](https://longgrovepharma.com/wp-content/uploads/2022/06/ab-rated-2.png)
The FDA evaluates generic drug products for therapeutic equivalence and assigns a code. The AB code means that the product was proven to be pharmaceutically equivalent and bioequivalent and can be substituted with the full expectation that it will have the same clinical effect and safety profile as the branded drug product.
![Carboprost is AP Rated Carboprost is AP Rated](https://longgrovepharma.com/wp-content/uploads/2022/08/ap-rated.png)
The FDA evaluates generic drug products for therapeutic equivalence and assigns a code. The AP code means that the product is an injectable aqueous solution and the information necessary to show bioequivalence between pharmaceutically equivalent products is either presumed or considered self-evident. The AP rated Long Grove generic is considered therapeutically equivalent to the branded drug product.