Aminosyn 4.25% W/ Dextrose 25% In Plastic Container
Amino Acids; Dextrose
Sourced from the FDA Orange Book
Key dates
Key dates
Approval
FDA approval date of this drug product.
Oct 11, 1984
42 yr 4 mo ago
Today
Pharmaceutical detail
Pharmaceutical detail
Active ingredient
AMINO ACIDS; DEXTROSE
Strength
4.25%;25GM/100ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
NDA 019119
Product number
001
Marketing status
Discontinued
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
This is a brand (NDA) product. Other products sharing this active ingredient are listed below.
- 1997Clinimix 2.75/10 Sulfite Free In Dextrose 10% In Plastic ContainerBrand (NDA)
NDA 020734 · Baxter Hlthcare
- 1988Aminosyn II 3.5% In Dextrose 25% In Plastic ContainerBrand (NDA)
NDA 019681 · Hospira
- 1988Travasol 2.75% In Dextrose 10% In Plastic ContainerBrand (NDA)
NDA 019520 · Baxter Hlthcare
- 1988Aminosyn II 3.5% In Dextrose 25% In Plastic ContainerBrand (NDA)
NDA 019713 · Abbott
- 1986Aminosyn II 5% In Dextrose 25% In Plastic ContainerBrand (NDA)
NDA 019565 · Abbott
- 1986Aminosyn II 3.5% In Dextrose 25% In Plastic ContainerBrand (NDA)
NDA 019505 · Abbott
- 1986Aminosyn II 3.5% In Dextrose 5% In Plastic ContainerBrand (NDA)
NDA 019506 · Abbott
- 1986Aminosyn II 4.25% In Dextrose 25% In Plastic ContainerBrand (NDA)
NDA 019504 · Abbott
- 1984Aminosyn 3.5% W/ Dextrose 25% In Plastic ContainerBrand (NDA)
NDA 019118 · Abbott
- 1984Aminosyn 3.5% W/ Dextrose 5% In Plastic ContainerBrand (NDA)
NDA 019120 · Abbott
Listed patents
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.
Aminosyn 4.25% W/ Dextrose 25% In Plastic Container — frequently asked questions
Approval, therapeutic equivalence, patents, and exclusivity for this product, from the FDA Orange Book.
Built directly from the FDA Orange Book data file. This product page links back to the Amino Acids; Dextrose active-ingredient family, which is the canonical reference for generics, patents, and exclusivity across all strengths.
Related FDA reference tools
- FDA Purple BookLicensed biologics, biosimilars, interchangeables, BLA records, and exclusivity dates.
- FDA BiosimilarsThe list of FDA-approved biosimilars and interchangeable biosimilars, by reference product.
- 510(k) Predicate DatabaseSearch FDA 510(k) clearances and map predicate-device lineage.
- FDA 483 & Inspection DatabaseFDA Form 483 observations and inspection records by firm, date, and citation.

