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Last Updated: March 29, 2024

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Dextrose - Generic Drug Details


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What are the generic drug sources for dextrose and what is the scope of patent protection?

Dextrose is the generic ingredient in one hundred and eighty-four branded drugs marketed by B Braun, Baxter Hlthcare, Fresenius Kabi Usa, Icu Medical Inc, Miles, Hospira, Abbott, DHL, and Intl Medication Sys, and is included in ninety-seven NDAs. Additional information is available in the individual branded drug profile pages.

There are nine drug master file entries for dextrose. Eleven suppliers are listed for this compound.

Summary for dextrose
Drug Prices for dextrose

See drug prices for dextrose

US Patents and Regulatory Information for dextrose

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Fresenius Kabi Usa DEXTROSE 5% AND SODIUM CHLORIDE 0.9% dextrose; sodium chloride INJECTABLE;INJECTION 211211-001 Sep 14, 2020 AP RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Abbott DEXTROSE 38.5% IN PLASTIC CONTAINER dextrose INJECTABLE;INJECTION 018923-001 Sep 19, 1984 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Baxter Hlthcare DEXTROSE 50% IN PLASTIC CONTAINER dextrose INJECTABLE;INJECTION 020047-001 Jul 2, 1991 AP RX Yes Yes ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Fresenius Kabi Usa POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.45% dextrose; potassium chloride; sodium chloride INJECTABLE;INJECTION 213523-005 Oct 11, 2022 AP RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Icu Medical Inc POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.225% IN PLASTIC CONTAINER dextrose; potassium chloride; sodium chloride INJECTABLE;INJECTION 018365-003 Jul 5, 1983 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
B Braun DEXTROSE 5% IN PLASTIC CONTAINER dextrose INJECTABLE;INJECTION 016730-002 Approved Prior to Jan 1, 1982 AP RX Yes Yes ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

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