View drug registration information details.

Items	Registration information
ID	9
No	9
Brand Name	DIGEKAM
Ingredients	DRIED ALUMINIUM HYDROXIDE GEL IH 300 MG, MAGNESIUM ALUMINIUM SILICATE HYDRATE IH 50 MG, MAGNESIUM HYDROXIDE BP 25 MG, SIMETICONE BP 25 MG
Dosage Form	CHEWABLE TABLETS
Primary Packaging	ALU-PVC BLISTER
Storage	STORE BELOW 30 C
Shelf Life	3 YEARS
Pack Size	BOX OF 10 X 15'S
Dispensing Category	PRESCRIPTION
ATC Classification
Pharmaceutical Class	ANTACID
Indications	FOR RELIEF OF SYMPTOMS HYPERACIDITY (E.G HEART BURN, EPIGASTRIC DISCOMFORT, OR THEIR EQUIVALENT) THAT ARE OFTEN ASSOCIATED WITH DYSPEPSIA, PEPTIC ULCER, GASTRITIS, PEPTIC ESOPHAGITIS, AND HIATUS HERNIA. IT IS ALSO INDICATED FOR RELIEF OF FLATULENCE.
Contraindications	HYPERSENSITIVITY
Side Effects	DIARRHEA, CONFUSION
Unit Price
EDL	No
Description	PINK COLORED, ROUND SHAPED, FLAT, UNCOATED CHEWABLE TABLET HAVING EMBOSSING DIGEKAM ON ONE SIDE AND PLAIN ON OTHER SIDE
Note
License Owner	ASA LAO SOLE COMPANY LIMITED
Manufacturer	IMPULSE PHARMA PVT. LTD
Country	INDIA
Import Registration No	KD641 (FORM 25)
Import Registration Date	2022-10-02
Activity	CERTIFICATE RELEASED
Applied Date	2024-02-23
FDD Registration No	01 I 5862/25
FDD Registration Date	2025-01-31
Expiry Date	2030-01-30

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