Bacopa Monnieri Extract

Bacopa Monnieri Extract


Negotiable Min Order Quantity Unit

Required Quantity
Place of Origin
India
Brand name
APEX BIOTECHNOL
Payment Terms
T/T
Production method
Negotiable
Shipping / Lead Time
Negotiable / Negotiable
Keyword
bacopa monnieri extract, bacosides
Category
Plant Extract
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APEX BIOTECHNOL

Membership
VIP
Country / Year Established
India India / 2015
Business type
Manufacturer
Verified Certificate

6

Product name Bacopa Monnieri Extract Certification -
Category Plant Extract Ingredients -
Keyword bacopa monnieri extract , bacosides Unit Size -
Brand name APEX BIOTECHNOL Unit Weigh 25 kg
origin India Stock -
Supply type - HS code -

Product Information

 

                                              Product Specifications

Product name

BacopaMonnieri Extract

Botanical name

BacopaMonnieri

Plant parts used

Whole Herb

Principal Constituents

Bacosides 50%

Country of Origin

India

Herb Ratio

30:1

Self-life 

3 years

Method

UV

 

Tested

Specifications

Method

A.      Physical Parameters

 

1.       Description

Light Brown color dry powder with characteristic odor

Visual /Organoleptic

2.       Identification

To comply by TLC

PP/QC/STP-GT/037

3.       Loss on drying

NMT 5.0%w/w

USP <731>

4.       Residue on Ignition

NMT 10.0%w/w

PP/QC/STP-TR/001

5.       Mesh size

100% passes through 40 mesh

USP <786>

6.       pH

5.0 – 7.0

USP

7.       Water soluble Extractives

NLT 75%

USP

8.       Tapped Bulk density

0.50 -1.0 g/ml

USP <616>

B.     Chemical Parameters

 

1.       Heavy Metal

NMT 10ppm

USP<2232>

Arsenic (As)

NMT 1.0ppm

ICP-OES

Lead (Pb)

NMT 3.0ppm

ICP-OES

Mercury (Hg)

NMT 0.1ppm

ICP-OES

Cadmium (Cd)

NMT 1.0 ppm

ICP-OES

Residual solvents

Should comply by ICH/USP

USP <467>

Residual Pesticides

Should comply by ICH/USP

USP <561>

2.       Active ingredient - Assay

 

 

Assay By UV Content of Total Bacosides

NLT 50.0% w/w on dry basis

 

PP/QC/STP- IN/023

C.        Microbiological Tests

 

1.       Total  Aerobic Plate Count

NMT 3000 cfu/g

USP <2021>

2.       Total Yeast &Mold

NMT 100Cfu/gm

USP <2021>

3.       E. coli

Absent /10g

USP <2022>

4.       Salmonella

Absent /10g

USP <2022>

5.       S. aureus

Absent /10g

USP <2022>

6.       Pseudomonas aeruginosa

Absent /10g

USP <62>

D.      Others

Packaging

Packed in Food grade HDPE Bags sealed into HDPE Containers

Storage

Air tight container, protect from heat & moisture

 

 

B2B Trade

Price (FOB) Negotiable transportation -
MOQ Negotiable Leadtime Negotiable
Payment Options T/T Shipping time Negotiable

APEX BIOTECHNOL

Country / Year Established
India India / 2015
Membership
VIP
Business type
Manufacturer

6

President
PRABHAT SINGH
Address
PLOT NO.303 ABHAYPUR INDUSTRIAL AREA PHASE 1 PANCHKULA
Product Category
Herbal Medicine
Year Established
2015
No. of Total Employees
1-50
Company introduction
<p>

Apex Biotechnol is an ISO 9001:2015, HACCP and a WHO-GMP certified company. We are working in the area of development of disease specific Herbal Extract and Enzymes solutions. With an unparalleled and unique combination of technical know-how, skilled resources and quality manufacturing, to open up exciting new avenues and offer products that surpass global standards. Apex Biotechnol's quality is ratified by its exports to USA, Europe, Japan, South Africa, Australia, etc. The company with its strong technical and marketing teams, extends unparalleled customer service and builds strong relationships.


We are a quality system for our manufacturing unit which makes us pioneers in providing better quality phytoextract product to our clients for other product requirements. Quality agreement and other processes which are a requirement for a smooth momentum of a manufacturing facility are maintained and complied. The research and development unit in our facility are utilized to test the product safety. Our suppliers of raw material also follow the Ethical code of conduct that are laid down by the FDA congruently produce an effective cutting edge finished product.


The guidance that we follow describes our current thinking on defining, establishing, and x-x-documenting the responsibilities that we lay on our suppliers and third party involved in the manufacturing of drugs with the subject to Current Good Manufacturing Practice (CGMP). In particular, we lay guidelines in the product manufacturing and describe how parties that are involved in the facility of preparing of drugs can follow and utilize Quality Agreements to delineate the responsibilities and assure drug quality, safety, and efficacy to the clients.

 

Main Markets

Germany Germany

Hong Kong(China) Hong Kong(China)

Indonesia Indonesia

North Korea North Korea

Russia Russia

Singapore Singapore

South Korea South Korea

Switzerland Switzerland

Thailand Thailand

Uzbekistan Uzbekistan

Factory Information

APEX BIOTECHNOL

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