DYSTOSEL DS INJECTION DIN 00682241
Status: Cancelled Post Market
Holder: PFIZER CANADA INC ANIMAL HEALTH GROUP
Molecule: SELENIUM (SODIUM SELENITE)
Health Canada record
| Active ingredient(s) | SELENIUM (SODIUM SELENITE) 6 MG; VITAMIN E (DL-ALPHA TOCOPHERYL ACETATE) 136 UNIT |
|---|---|
| Dosage form | Liquid |
| Route | Subcutaneous; Intramuscular |
| Schedule | NON-PRESCRIPTION DRUGS |
| Class | Veterinary |
| ATC | |
| Original market date | 31-Dec-1986 |
| Current status date | 17-Jul-2013 |
| Source | Health Canada DPD |
Establishment licence of the holder
Pfizer Canada ULC — licence 100255, currently licensed, last inspection rating C (2023-08-07).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing SELENIUM (SODIUM SELENITE)
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 00170968 | DYSTOSEL | ZOETIS CANADA INC | Emulsion | SELENIUM (SODIUM SELENITE) 3 MG; VITAMIN E (D-ALPHA TOCOPHERYL ACETATE) 136 UNIT | Marketed |
| 00518662 | E-SE INJECTABLE | INTERVET CANADA CORP | Solution | SELENIUM (SODIUM SELENITE) 2.5 MG; VITAMIN E (D-ALPHA TOCOPHERYL ACETATE) 68 UNIT | Marketed |
| 00518654 | MU-SE INJECTABLE | INTERVET CANADA CORP | Solution | SELENIUM (SODIUM SELENITE) 5 MG; VITAMIN E (D-ALPHA TOCOPHERYL ACETATE) 68 UNIT | Marketed |
| 01955551 | SELON-E | VETOQUINOL N A INC | Emulsion | SELENIUM (SODIUM SELENITE) 3 MG; VITAMIN E (DL-ALPHA TOCOPHERYL ACETATE) 136 UNIT | Marketed |
| 01940279 | E-SEL INJECTION | CITADEL ANIMAL HEALTH | Liquid | SELENIUM (SODIUM SELENITE) 3 MG; D-ALPHA TOCOPHERYL ACETATE 136 UNIT | Cancelled Post Market |
| 02229846 | FORMULA-SE | GESAR AG | Tablet | SELENIUM (SODIUM SELENITE) 30 MCG | Cancelled Post Market |
| 02046628 | NUTRISEL 200 PWR | HOFFMANN-LA ROCHE LIMITED | Powder | SELENIUM (SODIUM SELENITE) 200 MG | Cancelled Post Market |
| 02046601 | NUTRISEL 2000 PWR | HOFFMANN-LA ROCHE LIMITED | Powder | SELENIUM (SODIUM SELENITE) 2 G | Cancelled Post Market |
| 02016737 | SELENIUM - E | VETOQUINOL N A INC | Solution | SELENIUM (SODIUM SELENITE) 3 MG; VITAMIN E (DL-ALPHA TOCOPHERYL ACETATE) 136 UNIT | Cancelled Post Market |
| 00624772 | SELENIUM 10000 PREMIX 10000MG/KG | VAN WATERS AND ROGERS LTD. | Drug Premix | SELENIUM (SODIUM SELENITE) 10 G | Cancelled Post Market |
| 00714305 | SELENIUM PREMIX 100MG/KG | UNITED CO-OPERATIVES OF ONTARIO | Drug Premix | SELENIUM (SODIUM SELENITE) 100 MG | Cancelled Post Market |
| 02241722 | SELENIUM SUPPLEMENT | FOR MOR INTERNATIONAL INC. | Capsule | SELENIUM (SODIUM SELENITE) 30 MCG | Cancelled Post Market |
| 00364797 | SELEPHEROL INJECTION | BIMEDA-MTC ANIMAL HEALTH INC | Emulsion | SELENIUM (SODIUM SELENITE) 3 MG; VITAMIN E (DL-ALPHA TOCOPHERYL ACETATE) 136 UNIT | Dormant |
| 00753696 | SPECIAL PRESCRIPT SELEN PREMIX W COP & ZINC | LOVE FEEDS LTD. | Drug Premix | SELENIUM (SODIUM SELENITE) 1.05 MG; VITAMIN A 30000 UNIT; VITAMIN D3 3750 UNIT; VITAMIN E 5.25 UNIT; COPPER 50 MG; ZINC 150 MG | Cancelled Post Market |
| 00719072 | SPECTRUM 4 CAP | NF FORMULAS INC. | Capsule | SELENIUM (SODIUM SELENITE) 29.1 MCG; CHROMIUM (CHROMIC OXIDE) 33.3 MCG; ZINC (ZINC SULFATE) 1.16 MG; COPPER (COPPER GLUCONATE) .33 MG; MANGANESE (MANGANESE SULFATE) 1.66 MG; MOLYBDENUM (SODIUM MOLYBDATE) 8.3 MCG; CHOLINE BITARTRATE 8.3 MG; INOSITOL 8.3 MG; VITAMIN A (RETINOL PALMITATE) 1666.6 UNIT; BETA-CAROTENE 833.3 UNIT; VITAMIN E (DL-ALPHA TOCOPHERYL ACETATE) 66.6 UNIT; THIAMINE HYDROCHLORIDE 16.7 MG; VITAMIN B2 10 MG; NICOTINIC ACID 8.3 MG; NICOTINAMIDE 16.7 MG; D-PANTOTHENIC ACID (CALCIUM D-PANTOTHENATE) 25 MG; PYRIDOXINE HYDROCHLORIDE 25 MG; FOLIC ACID .133 MG; BIOTIN 33.3 MCG; ASCORBIC ACID (ASCORBIC ACID) 166.7 MG; VITAMIN B12 16.7 MCG; CALCIUM (CALCIUM CARBONATE) 58.3 MG; MAGNESIUM (MAGNESIUM OXIDE) 58.3 MG; IODINE (POTASSIUM IODIDE) .0375 MG; IRON (FERROUS FUMARATE) 3.3 MG; POTASSIUM (POTASSIUM CHLORIDE) 16.5 MG | Cancelled Post Market |
| 02230726 | SUPER-CELL | BODY WISE INTERNATIONAL LLC | Capsule | SELENIUM (SODIUM SELENITE) 50 MCG; VITAMIN E (D-ALPHA TOCOPHERYL ACID SUCCINATE) 15 UNIT; BETA-CAROTENE (PROVITAMIN A) 2500 UNIT; ASCORBIC ACID 25 MG; POTASSIUM (POTASSIUM CHLORIDE) 12.5 MG; MAGNESIUM (MAGNESIUM CITRATE) 25 MG; D-PANTOTHENIC ACID (CALCIUM D-PANTOTHENATE) 25 MG | Cancelled (Unreturned Annual) |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 6554 | 1999-07-06 | New Drug Submission (NDS) |