View drug registration information details.
Items | Registration information |
ID | 372 |
No | 372 |
Brand Name | ZINC SULFATE TABLETS USP 20 MG |
Ingredients | ZINC SULPHATE USP (AS MONOHYDRATE) 54.89 MG EQ.TO ELEMENTAL ZINC 20 MG |
Dosage Form | TABLET |
Primary Packaging | PVDC-ALU BLISTER |
Storage | STORE AT TEMPERATURE NOT EXCEEDING 30C IN A DRY PLACE, PROTECT FROM LIGHT, KEEP OUT OF REACH OFCHILDREN |
Shelf Life | 3 YEARS |
Pack Size | BOX OF 10 X 10'S |
Dispensing Category | Prescription only |
ATC Classification | A12CB01 |
Pharmaceutical Class | MINERAL SUPPLEMENT |
Indications | ZINC SULFATE IS INDICATED IN ADULT AND CHILDREN FOR THE TREATMENT OF ZINC DIFICIENCY |
Contraindications | HYPERSENSTIVITY TO ACTIVE SUBSTANCE, COPPER DEFICIENCY |
Side Effects | ABDOMINAL PAI, DYSPEPSIA, NAUSEA, VOMITING, DIARRHEA, GASTRIC IRRITATION AND GASTRITIS, |
Unit Price | |
EDL |
Yes |
Description | WHITE TO OFF WHITE, ROUND, FLATE, UNCOATED TABLET WITH BEVELED EDGES HAVING SCORE LINE ON ONE SIDE |
Note | |
License Owner | CBF PHARMA CO.,LTD |
Manufacturer | MEDICAMEN BIOTECH LIMITED |
Country | INDIA |
Import Registration No | 1127 |
Import Registration Date | 30/10/2007 |
Activity | CERTIFICATE RELEASED |
Applied Date | 2021-04-09 |
FDD Registration No | 10 I 5317/22 |
FDD Registration Date | 2022-11-11 |
Expiry Date | 2025-11-10 |
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