Ranitidine HCL IP active pharmaceutical ingredient

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Ranitidine HCL IP active pharmaceutical ingredient

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MOQ : 100 Kilograms

Ranitidine HCL IP active pharmaceutical ingredient Specification

Solubility
Freely soluble in water; slightly soluble in ethanol

Taste
Slightly bitter

Ph Level
5.5 - 7.0 (1% solution)

Molecular Weight
350.87 g/mol

Heavy Metal (%)
Not more than 0.001%

Storage
Store in a cool, dry place, protected from light

Poisonous
No under recommended use

Particle Size
D90 < 50 m

Color
White to pale yellow

Melting Point
140-144C

Smell
Odorless

Loss on Drying
Not more than 0.5%

HS Code
29349900

Boiling point
Not applicable (decomposes)

Molecular Formula
C13H22N4O3SHCl

EINECS No
266-566-1

Shelf Life
5 years from the date of manufacture if properly stored

Structural Formula
Available on request

Medicine Name
Ranitidine HCL IP

Chemical Name
N-(2-((5-((dimethylamino)methyl)furan-2-yl)methylthio)ethyl)-N-methyl-2-nitroethene-1,1-diamine hydrochloride

CAS No
66357-35-5

Type
Active Pharmaceutical Ingredient (API)

Grade
IP (Indian Pharmacopoeia) Grade

Usage
Used in the formulation of medicine for reducing stomach acid

Purity(%)
99% (min)

Appearance
White to pale yellow crystalline powder

Physical Form
Solid

Specific Optical Rotation
-52 to -58 (in water)

Chloride Content
Meets IP requirements

Residual Solvents
Complies with ICH guidelines

Related Substances
Total impurities: Not more than 0.5%

Identification
By IR, UV, and chemical methods conforming to standard

Assay (on anhydrous basis)
99% to 101%

Bacterial Endotoxins
<0.5 IU/mg

Total Plate Count
<1,000 cfu/g

Packing
Packed in HDPE Drum with double polyethylene liners or as per customer requirement

Manufacturing Standard
cGMP certified facility

Ranitidine HCL IP active pharmaceutical ingredient Trade Information

Minimum Order Quantity
100 Kilograms

Supply Ability
1000 Kilograms Per Week

Delivery Time
7 Days

Ranitidine HCL IP active pharmaceutical ingredient About

Grab the splendid opportunity to utilise our Ranitidine HCL IP, an impeccable active pharmaceutical ingredient crafted to the highest Indian Pharmacopoeia standards. With Specific Optical Rotation from -52 to -58 in water and assay purity between 99% to 101%, you won't want to miss this limited stock offer. Each batch is manufactured in a cGMP certified facility, ensuring controlled bacterial endotoxins and strict impurity limits. Secure your supply-packed securely in HDPE drums with double liners, this enlightened solution is ready to elevate your medicine formulation.

Applications of Ranitidine HCL IP

Ranitidine HCL IP finds its main area of application in the pharmaceutical industry, particularly in plant manufacturing settings, where it serves as a core ingredient in the formulation of acid-reducing medicines. The API is utilised at formulation plants and sites producing medications designed to manage gastric acid secretion. Its impeccable standards make it the preferred choice among medicine manufacturers and research facilities aiming for consistent, high-quality therapeutic effects.

Supply, Pricing, and Delivery Information

Our Ranitidine HCL IP is shipped promptly upon receipt of your proposal amount at the current sale price. Supply ability remains robust, catering to both small and bulk orders, with reliable global distribution. Expect swift delivery times, ensuring minimal waiting and efficient stock management. Payment terms are flexible to accommodate varied business needs, making procurement enjoyable and efficient for distributors, manufacturers, importers, and traders across India and beyond.

FAQ's of Ranitidine HCL IP active pharmaceutical ingredient:

Q: How should Ranitidine HCL IP be stored to maintain its quality?

A: Store Ranitidine HCL IP in a cool, dry place, protected from light, in order to preserve its quality and ensure a shelf life of up to 5 years from the date of manufacture.

Q: What is the main usage of Ranitidine HCL IP in pharmaceutical formulations?

A: Ranitidine HCL IP is primarily used as an active pharmaceutical ingredient for formulating medicines aimed at reducing stomach acid and treating related gastric disorders.

Q: Where is Ranitidine HCL IP commonly applied during manufacturing?

A: This API is commonly applied in pharmaceutical manufacturing plants, specifically at formulation and packaging sites where acid-reducing medications are produced.

Q: What are the benefits of using this specific grade of Ranitidine HCL IP?

A: The IP grade assures compliance with Indian Pharmacopoeia standards, offering impeccable purity, controlled impurities, and safety-ideal for high-quality medicine production.

Q: What process do you follow to ensure product quality and safety?

A: Ranitidine HCL IP is manufactured in a cGMP certified facility and goes through rigorous identification by IR, UV, and chemical tests to meet all regulatory and safety standards.