| ID | 390 |
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| No | 390 |
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| Brand Name | DOBUTAMINE - HAMELN 12.5 MG/ML INJECTION |
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| Ingredients | DOBUTAMINE HYDROCHLORIDE 14 MG/ML EQ.TO DOBUTAMINE 12.5 MG/ML |
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| Dosage Form | SOLUTION FOR INJECTION |
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| Primary Packaging | AMPOULES |
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| Storage | DO NOT STORE 25"C |
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| Shelf Life | 36 MONTHS FROM MANUFACTURING DATE |
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| Pack Size | BOX OF 5 AMPOULES X 20 ML |
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| Dispensing Category | Prescription only |
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| ATC Classification | C01CA07 |
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| Pharmaceutical Class | DOPAMINERGIC AGENT |
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| Indications | DOBUTAMINE IS INDICATED FOR PATIENTS WHO REQUIRE A POSITIVE INOTROPIC SUPPORT IN THE TREATMENT OF CARDIAC DECOMPENSATION DUE TO DEPRESSED CONTRACTILITY.IN CARDIOGENIC SHOCK CHARACTERISED BY HEART FAILURE WITH SEVERE HYPOTENSION. |
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| Contraindications | DOBUTAMINE MUST NOT BE USED IN THE CASE OF :
- KNOWN HYPERSENSITIVITY TO DOBUTAMINE OR TO ANY OF THE EXCIPIENTS |
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| Side Effects | EVALUATION OF UNDESIRABLE EFFECTS IS BASED ON THE FOLLOWING FREQUENCY SCALE : CARDIOVASCULAR. |
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| Unit Price | - |
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| EDL |
Yes |
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| Description | THE PRODUCT IS A CLEAR, COLOURLESS OR ALMOST COLOURLESS SOLUTION |
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| Note | |
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| License Owner | DAOVI PHARMA IMPORT-EXPORT SOLE CO.,LTD |
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| Manufacturer | SIEGFRIED HAMELN GMBH |
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| Country | GERMANY |
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| Import Registration No | 51613.01.00 |
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| Import Registration Date | 2004-04-23 |
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| Activity | CERTIFICATE RELEASED |
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| Applied Date | 2021-08-19 |
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| FDD Registration No | 11 I 4335/17 |
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| FDD Registration Date | 2022-05-17 |
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| Expiry Date | 2025-05-16 |
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