Diclofenac Sodium Injection IP

Name: Diclofenac Sodium Injection IP
Brand: UNIKA PHARMACEUTICALS PRIVATE LIMITED
Price: 3 INR
Availability: InStock

Price 3 INR/ Vial

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MOQ : 50 Vials

Diclofenac Sodium Injection IP Specification

Pacakaging (Quantity Per Box)
1 ml vial

Suitable For
Adults

HS Code
30049099

Purity
Pharmaceutical Grade

Assay
Not less than 98%

Dosage Guidelines
As directed by physician

CAS No
15307-79-6

Molecular Formula
C14H10Cl2NNaO2

Appearance
Clear colorless to faint yellow solution

Physical Form
Injection

Melting Point
296-298C (Diclofenac sodium)

Solubility
Freely soluble in water

Type
Pharmaceutical Injection

Ingredients
Diclofenac Sodium 25 mg/ml

Feature
IM or IV administration

Shelf Life
24 months

Storage Instructions
Store below 25C, protect from light

Brand Name
Dyclonac-AQ

Prescription
Required

Color of Box
Light Blue

Pack Size
1 ml

Strength
25 mg/ml

Regulatory Status
IP compliant

Box Contains
5 ampoules

Pack Type
Vial

Use
Analgesic

Route of Administration
IM or IV

Diclofenac Sodium Injection IP Trade Information

Minimum Order Quantity
50 Vials

Payment Terms
Cash in Advance (CID)

Supply Ability
5000 Vials Per Month

Delivery Time
2-5 Days

Main Domestic Market
All India

About Diclofenac Sodium Injection IP

Experience transcendent relief with Dyclonac-AQ, our Diclofenac Sodium Injection IP, formulated for effective analgesic action. Sourced from the finest pharmaceutical-grade ingredients, each 1 ml vial contains 25 mg/ml Diclofenac Sodium, delivering sublime performance for adult pain management. IP compliant and suitable for both IM and IV administration, it's available in a light blue box of 5 ampoules. Store below 25C to maintain purity. Explore this limited time offering and add it to your cart to ensure quality care when you need it most.

Targeted Analgesia for Effective Pain Management

Diclofenac Sodium Injection IP offers specific relief for acute pain and inflammatory conditions in adults, administered either intramuscularly or intravenously as directed by a physician. This clear, colorless to faint yellow solution provides rapid onset and consistent efficacy, making it a trusted choice in clinical and hospital settings. Its versatile application media ensures it can be easily integrated into various treatment protocols, delivering superior outcomes for pain management. Use with confidence for both moderate and severe pain indications.

Global Distribution and Reliable Shipping Solutions

We serve a wide export market, delivering Diclofenac Sodium Injection IP globally with secure shipping and robust logistics support. Our products are shipped from trusted FOB ports across India, ensuring efficient and safe delivery to our international clients. We offer samples upon request, allowing you to evaluate our quality firsthand. All consignments are handled with care to maintain product integrity, and orders are shipped promptly to meet your pharmaceutical supply chain demands.

FAQ's of Diclofenac Sodium Injection IP:

Q: How is Dyclonac-AQ Diclofenac Sodium Injection administered?

A: Dyclonac-AQ is administered to adults via intramuscular (IM) or intravenous (IV) injection, as prescribed by a licensed physician for the relief of pain and inflammation.

Q: What are the benefits of using Diclofenac Sodium Injection IP?

A: This injection provides targeted, rapid, and effective relief from acute pain and inflammatory conditions, ensuring quick onset and dependable outcomes in clinical practice.

Q: When should I use Diclofenac Sodium Injection IP?

A: Diclofenac Sodium Injection is indicated for use in moderate to severe pain scenarios, such as post-operative recovery, musculoskeletal injuries, or inflammatory conditions, when prescribed by a healthcare professional.

Q: Where is this injection exported from?

A: The Diclofenac Sodium Injection IP is securely shipped from India, utilizing reliable logistics networks and FOB ports to ensure safe international delivery.

Q: What process ensures the purity and quality of Dyclonac-AQ?

A: Each batch is prepared with pharmaceutical-grade raw materials, achieving not less than 98% assay purity, and is IP compliant. Product quality is further safeguarded by appropriate storage and stringent quality control measures.