Ranitidine HCL IP GMP certified manufacturer

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Ranitidine HCL IP GMP certified manufacturer

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MOQ : 100 Kilograms

Ranitidine HCL IP GMP certified manufacturer Specification

Particle Size
As per customer requirement (typically D90 150 m)

Solubility
Freely soluble in water, practically insoluble in chloroform and in ether.

Smell
Odorless

Color
Pale yellow to off-white

Melting Point
about 140C (decomposes)

Boiling point
Not applicable (decomposes before boiling)

Molecular Formula
C13H22N4O3S.HCl

Taste
Slightly bitter

Heavy Metal (%)
NMT 0.001%

Shelf Life
36 months from the date of manufacture

Poisonous
Non-poisonous under recommended usage

EINECS No
266-583-0

Loss on Drying
NMT 0.5%

Ph Level
5.5 - 6.5 (5% aqueous solution)

Molecular Weight
350.87 g/mol

Structural Formula
C13H22N4O3SHCl

HS Code
29335990

Storage
Store in a cool, dry and well-ventilated place, away from direct sunlight.

Medicine Name
Ranitidine HCL IP

Chemical Name
Ranitidine Hydrochloride

CAS No
66357-59-3

Type
Active Pharmaceutical Ingredient

Grade
IP (Indian Pharmacopoeia), GMP Certified

Usage
Used in the treatment of stomach ulcers, gastroesophageal reflux disease (GERD), and other conditions with excessive stomach acid.

Purity(%)
99% min.

Appearance
Off-white to pale yellow crystalline powder

Physical Form
Solid

Minimum Order Quantity
25 kg

Packaging Type
HDPE Drum / Double Polyliner Bag

Identification
IR, UV conform

Impurity Content
Complies with IP limits

Bacterial Endotoxins
Complies with pharmacopoeial standards

End Use Industry
Pharmaceuticals

Testing Method
Complies with IP specifications

Stability
Stable under recommended storage conditions

Ranitidine HCL IP GMP certified manufacturer Trade Information

Minimum Order Quantity
100 Kilograms

Supply Ability
1000 Kilograms Per Week

Delivery Time
7 Days

About Ranitidine HCL IP GMP certified manufacturer

Experience the dominant quality and astounding purity of our Ranitidine HCL IP, sought after for its impeccable standards in pharmaceutical manufacturing. Our GMP certified process yields an imposing, off-white to pale yellow crystalline powder with an assured 99% minimum purity, offered in HDPE Drums or Double Polyliner Bags. With stability under optimal storage and compliance with IP impurity limits, it's both safe and efficacious. This scarce and sizzling API is perfect for the treatment of ulcers and GERD-grab yours before supplies run out!

Optimal Plant Application and Usage Method

Our Ranitidine HCL IP is meticulously manufactured in GMP certified facilities, ensuring superior safety standards for pharmaceutical industries. Applications include its integration in solid, oral-dosage formulations, with precise measurement facilitated by customizable particle sizing. Intended primarily for pharmaceutical plants, this active ingredient is incorporated during the key stages of medicine production, following stringent IP compliance for maximum efficacy. Its stability and solubility design make it a versatile asset for large-scale pharmaceutical applications worldwide.

FOB Port, Packaging, and Delivery: Your Order's Journey

Your order of Ranitidine HCL IP is shipped efficiently from ports in India, with robust HDPE Drum or Double Polyliner Bag packaging for ultimate protection. Order processing begins promptly upon confirmation, ensuring swift preparation for export. We pride ourselves on responsive shipment schedules, and most deliveries arrive securely at your location within the targeted timeframe, subject to destination and order size. Unmatched reliability and transparency define each step, from order placement through to final delivery.

FAQ's of Ranitidine HCL IP GMP certified manufacturer:

Q: How is Ranitidine HCL IP typically used in pharmaceutical manufacturing?

A: Ranitidine HCL IP is predominantly used to formulate medications for treating stomach ulcers, gastroesophageal reflux disease (GERD), and related conditions. It is incorporated as an active ingredient in various oral pharmaceutical preparations, following GMP and IP guidelines.

Q: What makes your Ranitidine HCL IP stand out from competitors?

A: Our Ranitidine HCL IP offers an imposing combination of minimum 99% purity, strict GMP certification, stability, and compliance with the latest IP standards. Each batch is meticulously tested to ensure quality, safety, and potency, ensuring you receive a top-tier product.

Q: Where is the Ranitidine HCL IP produced and shipped from?

A: Our Ranitidine HCL IP is manufactured in India at GMP-compliant facilities and shipped from major Indian FOB ports. Packaging is robust to maintain product integrity during transit, and delivery is coordinated to meet client specifications.

Q: What is the typical shelf life and storage recommendation for Ranitidine HCL IP?

A: Ranitidine HCL IP boasts a shelf life of 36 months from its manufacturing date. It should be stored in a cool, dry, and well-ventilated area, away from direct sunlight, to ensure maximum stability and efficacy.

Q: How is product quality maintained during order processing and shipment?

A: Each order of Ranitidine HCL IP is securely packaged in HDPE Drum or Double Polyliner Bags and strictly complies with handling protocols. Orders are processed efficiently, and shipments are tracked to ensure timely and safe arrival at the client's destination.

Q: What are the benefits of partnering with your company as a Ranitidine HCL IP supplier?

A: By choosing us, you benefit from a GMP certified manufacturer, stringent quality controls, extensive packaging options, reliable global shipping, and responsive customer service-all designed to support the needs of the pharmaceutical industry.

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