Uses of Diclofenac Diethylamine, Methyl Salicylate Gel
Precautions for Diclofenac Diethylamine, Methyl Salicylate Gel
Systemic Risk: Avoid prolonged use over large skin areas to reduce the risk of systemic side effects.
Dosage Instructions As Follows:
Side Effects of Diclofenac Diethylamine, Methyl Salicylate Gel
Local Skin Reactions
These are usually mild and temporary, especially when applied to intact skin.
Allergic Reactions (Rare)
Discontinue use immediately if any allergic symptoms appear.
Systemic Effects (Uncommon but Possible)
Store below 30°C, preferably in a cool and dry place. Protect from light.
Keep the medicine out of reach of children.
Lami tube with a white cap containing 15 g of gel. Such a 01 tube in a unit carton with a pack insert.
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A pharma CMO is a special kind of an organization, offering contract manufacturing services to pharmaceutical companies for various kinds of drug formulations.
Reduce overall costs and time to market :
Contract manufacturers already have the needed infrastructure and technical staff, so working with a CMO or CDMO can decrease the cost of manufacturing your pharmaceutical products.
Scalability and flexible production capacity :
You can produce what you need when you need it without worrying about excess capacity. Additionally, CMOs understand the importance of quality and compliance, so you don't have to sacrifice safety for scalability.
Save on upgrading and maintaining equipment :
If you have your manufacturing facility, you’ll have to pay to upgrade your equipment as technology advances—which can get expensive. A CMO/CDMO’s only function is to make and distribute products, so part of their core business responsibility is to update their equipment whenever needed and perform maintenance.
Ease supply chain issues :
During the pandemic, there were several instances of supply chain issues, including medicine shortages. CMOs are generally better equipped than startups to handle a supply chain crisis.
Bandwidth to focus on core competencies
When your company resources aren’t directly allocated to manufacturing and distribution, you have more time to focus on other tasks, like marketing your new drug, researching, or working on drug discovery.
We have 7+ manufacturing sites with a minimum of WHO GMP certification and other country-specific approvals like NAFDAC approved, PPK Kenya Approved, TFDA Tanzania Approved, EU-GMP Approved.
We have below manufacturing capacity:
For Tablet, Capsule, and soft gel: up to 1 million units per shift
For Syrup: up to 0.05 Million per shift
For Ampoule and Vial: up to 0.1 million units per shift
For Ointment and Cream: up to 0.1 million units per shift
For Suppository: 0.1 Million units per shift
