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NAD+

Healthcare Provider Pricing

Pricing is available exclusively for verified medical providers.

Daulcél NAD⁺ for Injection is a pharmaceutical-grade, sterile lyophilized formulation of β-Nicotinamide Adenine Dinucleotide (oxidized form), supplied in a single-use 500 mg vial for intravenous administration by qualified healthcare professionals.

NAD⁺ is a critical intracellular coenzyme essential for mitochondrial ATP production, DNA repair, and activation of sirtuin pathways that regulate cellular aging. Declining NAD⁺ levels are strongly associated with impaired cellular repair mechanisms, oxidative stress accumulation, and visible biological aging of the skin.


• 500 mg NAD+ (Lyophilized Cake Form)
• Sterile single-use vial
• For IV administration only


Cellular Longevity Begins Within.

REQUEST ACCESS FOR NAD+

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Cellular Dossier Visualization

Molecular Architecture

Engineered to maintain molecular stability and integrity of β-Nicotinamide Adenine Dinucleotide during clinical preparation and administration.

ATP Synthesis Induction

Participates in essential redox reactions and mitochondrial pathways involved in cellular ATP production and metabolic function.

Sirtuin Activation

Serves as a critical cofactor for sirtuin enzymes associated with cellular repair, mitochondrial regulation, and healthy aging pathways.

Clinical Protocol

Guidelines and pharmaceutical specifications for licensed healthcare providers.

SUPPLY FORMAT
Sterile single-use 500mg vial.
ADMINISTRATION
For intravenous (IV) administration only by qualified healthcare professionals.
RECONSTITUTION
Requires reconstitution with specific volumes of sterile Normal Saline (0.9% NaCl) or Bacteriostatic Water prior to infusion.
STORAGE
Store intact vials at controlled room temperature. Protect from light. Refrigerate and use within specified clinical timelines.

Uncompromising Quality

Manufactured to exact pharmaceutical tolerances. Every vial guarantees absolute stability, purity, and clinical efficacy.

PHASE // 01

WHO-GMP Manufacturing

Manufactured in WHO-GMP compliant facilities under strictly controlled sterile environments to ensure pharmaceutical-grade quality and molecular integrity.

PHASE // 02

Lyophilization Protocol

Our formulas undergo precise freeze-drying processes to lock in absolute potency and ensure maximum stability until the exact moment of clinical reconstitution.

PHASE // 03

Analytical Verification

Every batch undergoes sterility and stability testing and is accompanied by a batch-specific Certificate of Analysis (COA) to verify purity, concentration, and quality compliance.