FENUGREEK SEED DIN 02239980
Health Canada record
| Active ingredient(s) | FENUGREEK 600 MG |
|---|---|
| Dosage form | Tablet |
| Route | Oral |
| Schedule | NON-PRESCRIPTION DRUGS |
| Class | Human |
| ATC | |
| Original market date | 01-Jun-1999 |
| Current status date | 31-Jul-2002 |
| Source | Health Canada DPD |
Establishment licence of the holder
Vita Health Products Inc. — licence 100399, currently licensed, last inspection rating C (2025-03-03).
No Canadian shortage report is currently matched to this DIN.
International API supply for FENUGREEK
1 active FDA Drug Master Files.
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