Drug · DIN 02237039
CENTRUM TABLETS
No: no longer authorized
The company stopped selling it and its DIN was cancelled. A cancellation is most often a business decision; the record does not say why.
Status Cancelled Post Market since October 3, 2003; first marketed September 21, 1998.
- Drug Identification Number (DIN)
- 02237039
- Company (DIN owner)
- Whitehall-Robins Inc.Mississauga, Ontario, Canada
- Schedule
- Non-prescription drugs
- Dosage form
- Tablet
- Route
- Oral
- Therapeutic class (ATC)
- Multivitamins and other minerals incl combinations A11AA03
- Class
- Human
- Record last updated
- March 22, 2025
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| BETA-CAROTENE | 3000 UNIT | |
| VITAMIN A (VITAMIN A ACETATE) | 2000 UNIT | |
| VITAMIN E (DL-ALPHA TOCOPHERYL ACETATE) | 25 UNIT | |
| ASCORBIC ACID (ASCORBIC ACID) | 90 MG | |
| FOLIC ACID | 0.4 MG | |
| VITAMIN B1 (THIAMINE MONONITRATE) | 2.25 MG | |
| VITAMIN B2 (VITAMIN B2) | 3.2 MG | |
| NICOTINAMIDE | 40 MG | |
| VITAMIN B6 (PYRIDOXINE HYDROCHLORIDE) | 3 MG | |
| VITAMIN B12 (VITAMIN B12) | 14 MCG | |
| VITAMIN D (VITAMIN D3) | 400 UNIT | |
| BIOTIN | 45 MCG | |
| D-PANTOTHENIC ACID (CALCIUM D-PANTOTHENATE) | 10 MG | |
| CALCIUM (CALCIUM PHOSPHATE (DIBASIC), CALCIUM CARBONATE) | 175 MG | |
| PHOSPHORUS (CALCIUM PHOSPHATE (DIBASIC)) | 125 MG | |
| IODINE (POTASSIUM IODIDE) | 150 MCG | |
| IRON (FERROUS FUMARATE) | 10 MG | |
| MAGNESIUM (MAGNESIUM OXIDE) | 50 MG | |
| COPPER (CUPRIC OXIDE) | 2 MG |
Other DINs named CENTRUM TABLETS
- DIN 02166666 · Cancelled Post Market