HAIR REGROWTH FORMULA DIN 02356597
Health Canada record
| Active ingredient(s) | MINOXIDIL 20 MG |
|---|---|
| Dosage form | Solution |
| Route | Topical |
| Schedule | NON-PRESCRIPTION DRUGS |
| Class | Human |
| ATC | D11AX01 MINOXIDIL, TOPICAL |
| Original market date | 15-Apr-2011 |
| Current status date | 15-Apr-2011 |
| 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.
Other Canadian products containing MINOXIDIL
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02460181 | HAIR REGROWTH TREATMENT | APOTEX INC | Solution | MINOXIDIL 2 % | Approved |
| 00514500 | LONITEN 10MG | PFIZER CANADA ULC | Tablet | MINOXIDIL 10 MG | Marketed |
| 00514497 | LONITEN 2.5MG | PFIZER CANADA ULC | Tablet | MINOXIDIL 2.5 MG | Marketed |
| 02553465 | MEN'S GLN-MINOXIDIL | GLENMARK PHARMACEUTICALS CANADA INC. | Aerosol (Foam) | MINOXIDIL 5 % | Marketed |
| 02551446 | MEN’S HAIR REGROWTH TREATMENT | TARO PHARMACEUTICALS INC | Aerosol (Foam) | MINOXIDIL 5 % | Marketed |
| 00708925 | MEN'S ROGAINE | KENVUE CANADA INC. | Solution | MINOXIDIL 20 MG | Marketed |
| 02368684 | MEN'S ROGAINE FOAM 5% | KENVUE CANADA INC. | Aerosol (Foam) | MINOXIDIL 5 % | Marketed |
| 02570300 | MINOXIDIL 5% MEN / HOMMES | NORA PHARMA INC | Aerosol (Foam) | MINOXIDIL 5 % | Approved |
| 02555980 | WOMEN'S GLN-MINOXIDIL | GLENMARK PHARMACEUTICALS CANADA INC. | Aerosol (Foam) | MINOXIDIL 5 % | Approved |
| 02551659 | WOMEN'S HAIR REGROWTH TREATMENT | TARO PHARMACEUTICALS INC | Aerosol (Foam) | MINOXIDIL 5 % | Marketed |
| 02424703 | WOMEN'S ROGAINE FOAM 5% | KENVUE CANADA INC. | Aerosol (Foam) | MINOXIDIL 5 % | Marketed |
| 00885754 | APO-GAIN LIQ 20MG/ML | APOTEX INC | Solution | MINOXIDIL 20 MG | Dormant |
| 02065800 | GEN-MINOXIDIL LIQ 2% | GENPHARM ULC | Liquid | MINOXIDIL 2 % | Cancelled Post Market |
| 02242377 | HAIR REGROWTH TREATMENT | VITA HEALTH PRODUCTS INC | Solution | MINOXIDIL 2 % | Cancelled Post Market |
| 02242376 | HAIRGRO | VITA HEALTH PRODUCTS INC | Solution | MINOXIDIL 2 % | Cancelled Post Market |
| 02529238 | JAMP MINOXIDIL SOLUTION | JAMP PHARMA CORPORATION | Solution | MINOXIDIL 20 MG | Dormant |
| 02228319 | MINOX | LABORATOIRE RIVA INC. | Solution | MINOXIDIL 20 MG | Dormant |
| 02146835 | MINOXIGAINE TOPICAL SOLUTION - 2% | ALTIMED PHARMA INC. | Solution | MINOXIDIL 20 MG | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 29849 | 2023-01-05 | Supplement to a New Drug Submission (SNDS) | Labelling Update (to Match Licensor) |
| 24447 | 2020-10-16 | Supplement to a New Drug Submission (SNDS) | LABELLING UPDATE TO MATCH LICENSOR |
| 11724 | 2010-09-21 | New Drug Submission (NDS) | New manufacturer and product name |
International API supply for MINOXIDIL
11 valid EDQM Certificates of Suitability from 11 holders. 10 active FDA Drug Master Files.
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