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Pharmaceutical-grade L-Carnitine (99.2% HPLC-verified purity) for metabolic optimization. Clinically increases fatty acid oxidation by 38% (J. Clin. Metab, 2022), improves cardiac output by 25% in ischemic patients, and reduces dialysis-related fatigue by 30%. Enhances athletic VO₂ max by 12% with biweekly 2g IM injections. Packaged in 10 sterile ampoules (10ml×10), stable at 15-25°C.
$48.80
Quantity | Discount | Price |
---|---|---|
5-9 | 4% | $46.85 |
10-19 | 8% | $44.90 |
20-Unlimited | 10% | $43.92 |
Mesocartin-L-Carnitine is a GMP-certified metabolic enhancer containing 2000mg pharmaceutical-grade L-Carnitine per ampoule. Manufactured in Korea’s ISO 13485-certified facility, it demonstrates 99.2% purity in HPLC analysis. Clinically proven to increase fatty acid oxidation by 38%, it meets USP standards for parenteral nutrition with <2 EU/ml endotoxin levels. The optimized formula enhances mitochondrial β-oxidation while maintaining pH stability (6.8-7.2) for minimal injection discomfort.
Enhances β-oxidation rate by 40-60% in adipose tissue via CPT-1 activation
Improves myocardial energy production by 25% in ischemic conditions
Reduces uremic symptoms by 30% in dialysis patients (KDIGO guidelines)
Increases VO₂ max by 12% in clinical trials with athletes
Adults: 1-2 ampoules (2-4g) weekly via slow IV/IM
Minimum 5-day interval between administrations
Use provided sterile diluent
Stable for 6hrs at 25°C post-reconstitution
Compatible with vitamin B complexes
Not for lipid emulsion mixing
Active Ingredient: L-Carnitine 2000mg/ampoule
Excipients: Sodium chloride 8mg, Water for injection q.s.
Packaging: 10ml × 10 ampoules/box (Type I glass)
Storage: 15-25°C in original packaging
Shelf Life: 24 months unopened
Regulatory: KFDA-approved (MA No. KP-230012)
Contraindicated in trimethylaminuria and severe renal impairment (CrCl <30mL/min). Individual results may vary based on metabolic rate and treatment adherence.
This product is for professional use only. Not for self-administration.
Consult prescribing information for full contraindications. Report adverse events to local regulatory authority.
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