View drug registration information details.
Items | Registration information |
ID | 142 |
No | 142 |
Brand Name | SIRMOX-CL 228.5 |
Ingredients | EACH 5 ML CONTAINS: AMOXICILLIN TRIHYDRATE USP EQ.TO AMOXICILLIN 200 MG, DILUTED POTASSIUM CLAVULANATE BP EQ.TO CLAVULANIC ACID 28.5 MG. |
Dosage Form | SUSPENSION |
Primary Packaging | BOTTLE |
Storage | STORE BELOW 30 C |
Shelf Life | 2 YEARS |
Pack Size | 100 ML/BOTTLE |
Dispensing Category | PRESCRIPTION |
ATC Classification | |
Pharmaceutical Class | ANTIBACTERIAL COMBINATIONS |
Indications | ACUTE BACTERIAL SINUSITIS, ACUTE OTITIS MEDIA, ACUTE EXACERBATIONS OF CHRONIC BRONCHITIS, COMMUNITY ACQUIRED PNEUMONIA, CYSTITIS, PYELONEPHRITIS, SKIN AND SOFT TISSUE INFECTION, BONE AND JOINT INFECTION. |
Contraindications | HISTORY OF SEVERE IMMEDIATED HYPERSENSITIVITY REACTION, HISTORY OF JAUNDICE/HEPATIC IMPAIRMENT DUE TO AMOXICILLIN/CLAVULANCI ACID |
Side Effects | MUCOCUTANEOUS CANDIDOSIS, DIARRHEA, NAUSEA, VOMITING, |
Unit Price | |
EDL |
Yes |
Description | A WHITE TO PALE YELLOW COLORED FREE FLOWING POWDER GIVES YELLOW COLORED SUSPENSION AFTER ADDITION OF WATER. |
Note | |
License Owner | ASA LAO SOLE COMPANY LIMITED |
Manufacturer | KRUX PHARMA PVT.LTD |
Country | INDIA |
Import Registration No | G/28/1714 |
Import Registration Date | 28.10.2020 |
Activity | CERTIFICATE RELEASED |
Applied Date | 2022-09-09 |
FDD Registration No | 04 I 5459/23 |
FDD Registration Date | 2023-04-11 |
Expiry Date | 2026-04-10 |
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