L-Carnitine

Also known as · Levocarnitine · Carnitor · ALC (acetyl form)

01 / Dosing schedule

Cited dosing

The FDA-approved Carnitor injection is for IV use only, dosed for acute or chronic treatment of primary and secondary carnitine deficiency. Oral Carnitor is dosed at 990 mg two to three times daily.

Carnitor injection — IV use, deficiency

PhaseDose & frequency
Adult dose50 mg/kg IV as a loading dose, followed by 50 mg/kg/day (max ~5 g/day) infused
RouteIntravenous only — label is explicit
Vial1 g levocarnitine per 5 mL
Half-lifeTerminal ~17.4 h; distribution ~35 min

Source · FDA label — Carnitor injection (2018) ↗

Carnitor oral — adult deficiency

PhaseDose & frequency
Standard oral dose990 mg (three 330 mg tablets) two to three times daily
Alternative oral solution1–3 g/day (10–30 mL/day) for a 50 kg subject
RouteOral only — not parenteral

Source · FDA label — Carnitor oral (2002) ↗

Source indication · Primary systemic carnitine deficiency and secondary deficiency in patients on hemodialysis (Carnitor label).

Injection frequency
IV: daily infusion. Oral: two to three times daily.
Injection sites
IV: central or peripheral line per protocol.

02 / Reconstitution

Reconstitution reference

Carnitor injection ships pre-formulated as 1 g per 5 mL (200 mg/mL) — no reconstitution required. For research-grade L-carnitine powder, a typical prep is 1 g in 4 mL bacteriostatic water = 250 mg/mL. The FDA label restricts injection to IV use; other parenteral routes are outside the label.

Vial1 g
BAC water5 mL (pre-formulated) or 4 mL BAC water (research)
Concentration200 mg/mL (label) or 250 mg/mL (research)
Example dose500 mg
On a U‑100 syringe2.5 mL (label) or 2 mL (research)
Open the reconstitution calculator →

03 / Overview

Protocol overview

L-Carnitine (levocarnitine) is an endogenous carrier that shuttles long-chain fatty acids across the inner mitochondrial membrane for beta-oxidation.

The FDA-approved indications are primary systemic carnitine deficiency and secondary carnitine deficiency in patients on chronic hemodialysis. The label is explicit that the injection is for IV use only.

The terminal plasma half-life after IV administration is ~17.4 hours. Roughly 76% of an IV dose is excreted in the urine within 24 hours in patients with normal renal function.

Bodybuilding and metabolic-research protocols using intramuscular or subcutaneous injection are outside the FDA label. The label limits parenteral use to intravenous administration.

04 / References

References

  1. FDA prescribing information — Carnitor injection 2018 ↗
  2. FDA prescribing information — Carnitor oral 2002 ↗