Treats an inborn error of metabolism. ANDA 217896, held by Baxter Hlthcare Corp. Levocarnitine.
As of Nov 13, 2026, ANDA 217896 (Levocarnitine), held by Baxter Hlthcare Corp, was first approved by FDA on Jul 2, 2026, with 0 approved supplements and 0 published complete response letters.
INDICATIONS AND USAGE For the acute and chronic treatment of patients with an inborn error of metabolism which results in secondary carnitine deficiency. For the prevention and treatment of carnitine deficiency in patients with end stage renal disease who are undergoing dialysis.
| Date | Submission | Status | Documents |
|---|---|---|---|
| Jul 2, 2026 | Original application | Approved | None posted |
| Product | Active ingredient | Marketing |
|---|---|---|
| Levocarnitine200MG/ML · injectable;injection | Levocarnitine | Rx |
Approvals, supplements, products and documents come from FDA's Drugs@FDA data files, refreshed daily; Drugs@FDA lists approved applications only. Complete response letters are FDA's published letters. Drugs@FDA and FDA complete response letters
