CUPRIMINE DIN 00016055
Health Canada record
| Active ingredient(s) | PENICILLAMINE 250 MG |
|---|---|
| Dosage form | Capsule |
| Route | Oral |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | M01CC01 PENICILLAMINE |
| Original market date | 31-Dec-1964 |
| Current status date | 13-Dec-2019 |
| Source | Health Canada DPD |
Establishment licence of the holder
Bausch Health Companies Inc. — licence 101880, currently licensed, last inspection rating C (2026-06-01).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing PENICILLAMINE
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 00497894 | CUPRIMINE | MERCK CANADA INC | Capsule | PENICILLAMINE 125 MG | Cancelled Post Market |
| 00511641 | DEPEN TAB 250MG | CARTER-HORNER CORP. | Tablet | PENICILLAMINE 250 MG | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 23014 | 2019-12-13 | New Drug Submission (NDS) | CHANGE IN PRODUCT OWNERSHIP. UPDATE TO THE PRODUCT MONOGRAPH, PACKAGE INSERT AND LABELS |
| 13144 | 2012-03-26 | New Drug Submission (NDS) | Manufacturer name change |
| 9008 | 2007-09-06 | New Drug Submission (NDS) | MANUFACTURER NAME CHANGE |
| 7095 | 2005-06-17 | New Drug Submission (NDS) | MANUFACTURER NAME CHANGE |
International API supply for PENICILLAMINE
3 valid EDQM Certificates of Suitability from 3 holders. 11 active FDA Drug Master Files.
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