Human Formulations

Lansoprazole IP 30 mg (As Enteric Coated Granuels) + Domperidone lpP 10 mg (As Coated Pellets) Capsules

Lansoprazole IP 30 mg (As Enteric Coated Granuels) + Domperidone lpP 10 mg (As Coated Pellets) Capsules is a capsule formulated with Lansoprazole IP 30 mg (As Granuels) + Domperidone lpP 10 mg (As Coated Pellets). The listed active ingredient profile is L

CapsulesNon-Beta-Lactam Capsules Single Ingredient Capsule
Sterile injectable formulation

Product information

Product Line
Human Formulations
Category
Capsules, Non-Beta-Lactam Capsules
Dosage Form
Capsule
Product Type
Single Ingredient

Available strengths

Lansoprazole IP 30 mg (As Granuels) + Domperidone lpP 10 mg (As Coated Pellets)

Description

Lansoprazole IP 30 mg (As Enteric Coated Granuels) + Domperidone lpP 10 mg (As Coated Pellets) Capsules is a capsule formulated with Lansoprazole IP 30 mg (As Granuels) + Domperidone lpP 10 mg (As Coated Pellets). The listed active ingredient profile is Lansoprazole; Domperidone lpP, placing the product in the gastrointestinal / acid-peptic therapy category. The formulation contains acid-suppressive and/or prokinetic components used in selected gastrointestinal conditions. The source indicates enteric coated characteristics, which should be retained exactly because release technology can affect administration and product performance. For website cataloguing, the composition, strength, dosage form and formulation characteristics should be displayed prominently and consistently. The product description should remain factual and should not include unapproved cure, superiority, guaranteed-result or broad therapeutic claims. Clinical selection should depend on diagnosis, patient-specific factors, contraindications, concomitant medicines and professional judgement. Prescription status, warnings, interactions, adverse effects and dosing or application instructions must be checked against the current approved product label. Manufacturer, licence, storage, shelf-life, reconstitution where applicable, and market-specific regulatory details should be added only from verified product documentation.
WHO-GMP Sourced
Sterile Supply
Regulatory Documentation
Quality Assured