View drug registration information details.
Items | Registration information |
ID | 7 |
No | 7 |
Brand Name | CLOPIGREL 75 |
Ingredients | CLOPIDROGREL BISULFATE USP EQ.TO CLOPIDROGREL 75 MG |
Dosage Form | FILM COATED TABLET |
Primary Packaging | ALU-ALU BLISTER |
Storage | STORE BELOW 30 C |
Shelf Life | 3 YEARS |
Pack Size | BOX OF 10 X 10'S |
Dispensing Category | PRESCRIPTION |
ATC Classification | |
Pharmaceutical Class | ANTIPLATELET |
Indications | ADULT PATIENTS SUFFERING FROM MYOCARDIAL INFARCTION, ISCHAEMIC STROKE (FROM 7 DAYS UNTIL LESS THAN 6 MONTHS OR ESTABLISHED PERIPHERAL ARTERIAL DISEASE. ADULT PATIENTS SUFFERING FROM ACUTE CORONARY SYNDROME, NON-ST SEGMENT ELEVATION ACUTE CORONARY SYNDROME INCLUDING PATIENTS UNDERGOING A STENT PLACEMENT FOLLOWING PERCUTANEOUS CORONARY INTERVENTION, IN COMBINATION WITH ACETYLSALICYLIC ACID. |
Contraindications | HYPERSENSITIVITY, SEVERE HEPATIC IMPAIRMENT, ACTIVE PATHOLOGICAL BLEEDING SUCH AS PEPTIC ULCER OR INTRACRANIAL HAEMORRHAGE. |
Side Effects | TASTE DISORDERS, VASCULITIS, HYPOTENSION, SKIN BLEEDING, SERUM SICKNESS, ABNORMAL LIVER FUNCTION TEST, ACUTE LIVER FAILURE. |
Unit Price | |
EDL |
Yes |
Description | BROWN COLORED, CIRCULAR SHAPED, BICONVEX, FILM COATED TABLET, PLAIN ON BOTH SIDES |
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 5861/25 |
FDD Registration Date | 2025-01-31 |
Expiry Date | 2030-01-30 |
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