NDC 63323-712 – Kabiven

Dextrose Monohydrate 10.8 g/100mL; Soybean Oil 3.9 g/100mL; Sodium Acetate 239 mg/100mL; Potassium Chloride 174 mg/100mL; Sodium Glycerophosphate Anhydrous 147… · Injection, Emulsion · Intravenous

Human Prescription Drug 1 recall

Product NDC63323-712

Product details

Brand name
Kabiven
Generic name
Dextrose, Soybean oil, Electrolytes, Lysine, Phenylalanine, Leucine, Valine, Threonine, Methionine, Isoleucine, Tryptophan, Alanine, Arginine, Glycine, Proline, Histidine, Glutamic Acid, Serine, Aspartic Acid and Tyrosine
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection, Emulsion
Route
Intravenous
Marketing category
NDA · NDA200656
Marketed since
August 25, 2014
Listing expires
December 31, 2026
Pharmacologic class
Amino Acid; Blood Coagulation Factor; Calculi Dissolution Agent; Lipid Emulsion; Osmotic Laxative; Osmotic Laxative; Osmotic Laxative; Osmotic Laxative; Phosphate Binder; Potassium Salt

Active ingredients

Uses, dosage, side effects and warnings for Kabiven →

Package NDC codes (4)

Package NDCDescriptionSince
63323-712-101026 mL in 1 BAG (63323-712-10)Aug 25, 2014
63323-712-151540 mL in 1 BAG (63323-712-15)Aug 25, 2014
63323-712-202053 mL in 1 BAG (63323-712-20)Aug 25, 2014
63323-712-252566 mL in 1 BAG (63323-712-25)Aug 25, 2014

Recalls mentioning this NDC