GMP Nicotinic Acid Injection 1%/1ml 10mg/1ml

Product Details
Customization: Available
Application: Internal Medicine
Usage Mode: for Injection
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Management System Certification
ISO 9001, ISO 9000, GMP, HACCP, BREEAM
Export Year
2016-07-01
  • GMP Nicotinic Acid Injection 1%/1ml 10mg/1ml
  • GMP Nicotinic Acid Injection 1%/1ml 10mg/1ml
  • GMP Nicotinic Acid Injection 1%/1ml 10mg/1ml
  • GMP Nicotinic Acid Injection 1%/1ml 10mg/1ml
  • GMP Nicotinic Acid Injection 1%/1ml 10mg/1ml
  • GMP Nicotinic Acid Injection 1%/1ml 10mg/1ml
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Basic Info.

Model NO.
SINOHM2476
Suitable for
Elderly, Children, Adult
State
Liquid
Shape
Injection
Type
Biological Products
Pharmaceutical Technology
Chemical Synthesis
Function
Pellagra Treatment,Antioxidant,Vasodilation,Dermat
Group
All Age Ranges
Certification
CE, FDA, EEC, MSDS, GMP
Quality Guarantee Period
Three Years
Store Method
Normal Temperature
Main Ingredient
Nicotinic
Formula
Ultra Strength
Quality Control
European or Us-FDA Standard
Usage
Intramuscular Injection,Intravenous Injection
MOQ
5000 Boxes
OEM Service
Available
Registration Dossiers
Available
Factory Inspection
Available
Sample
Available
Route
Injection
Transport Package
10 Vials+10 AMPS/Box, 5 Vials+5 AMPS/Box
Specification
1%/1ml 10mg/1ml
Trademark
SUPER GLUTA
Origin
China
HS Code
3004909099
Production Capacity
1, 000, 000 Vials + 1, 000, 000 Ampoules/Month

Product Description

PRODUCT NAME: (New) SUPER GLUTA® (Nicotinic Acid Injection 10mg1ml)
STRENGTH: 1%/1ml   10mg/1ml
PACKING DETAILS: 10 Ampoules /box
STORAGE: Store in a cool and dry place below 25ºC, protected from light.
SHELF LIFE: 36 months
REGISTRATION DOSSIERS ARE AVAILABLE.
CONSIGNMENT MANUFACTURING, BRAND OEM/ODM SERVICE IS AVAILABLE.
 

1. Skin Barrier Repair & Anti-Aging 

Nicotinamide injection demonstrates remarkable dermatological benefits by enhancing skin barrier function and mitigating signs of aging. As a precursor to NAD+, it boosts cellular energy metabolism in keratinocytes, accelerating the synthesis of ceramides and filaggrin-key components for moisture retention. Clinical studies indicate its efficacy in reducing transepidermal water loss (TEWL) by up to 30%, making it valuable for treating xerosis (pathologically dry skin).

Additionally, its anti-inflammatory properties suppress cytokines like IL-6 and TNF-α, alleviating conditions like acne and rosacea. Topical applications are more common, but systemic administration via injection may benefit severe cases (e.g., post-chemotherapy skin toxicity). A 2022 Journal of Investigative Dermatology study noted 25% improvement in skin elasticity with high-dose nicotinamide regimens.

 

2. Pellagra Treatment 

Nicotinamide injection is a first-line therapy for pellagra, a life-threatening niacin deficiency disease. It rapidly replenishes NAD/NADP pools, reversing the classic triad of dermatitis, diarrhea, and dementia. Unlike nicotinic acid, it avoids vasodilation-induced flushing, making it safer for acute care.

The WHO recommends 300-500 mg/day IV/IM for severe cases, with symptom resolution within 48 hours. A 2020 meta-analysis confirmed 92% efficacy in resolving neurological symptoms when administered early. Contraindications include concurrent isoniazid use (competes for metabolic pathways).

 

3. Diabetic Neuropathy Adjunct 

By improving microvascular circulation and reducing oxidative stress, nicotinamide injection aids in managing diabetic peripheral neuropathy (DPN). It preserves neuronal function via NAD+-dependent SIRT1 activation, which mitigates mitochondrial dysfunction.

Trials show 200 mg/day IV for 12 weeks reduces neuropathic pain scores by 40% (Diabetes Care, 2021). However, it's adjunctive to standard therapies (e.g., alpha-lipoic acid). Caution is needed in renal impairment due to potential hyperphosphatemia risk.

 

4. Chemo-Radiotherapy Support 

Nicotinamide injection mitigates mucositis and dermatitis induced by cancer therapies. It enhances DNA repair via PARP-1 upregulation and reduces radiation-induced fibrosis.

A phase III trial (Lancet Oncology, 2023) demonstrated 50% lower grade 3-4 oral mucositis incidence with prophylactic IV nicotinamide (500 mg/m²). It's often combined with glutamine infusions. Note: Benzyl alcohol-free formulations are critical for pediatric oncology use.



We are looking for the SUPER GLUTA® agents all around the world.
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Moreover, kindly note that we are always providing our customers with Consignment Manufacturing Serivce, OEM/ODM.

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