LONITEN 2.5MG DIN 00514497
Health Canada record
| Active ingredient(s) | MINOXIDIL 2.5 MG |
|---|---|
| Dosage form | Tablet |
| Route | Oral |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | C02DC01 MINOXIDIL |
| Original market date | 31-Dec-1980 |
| Current status date | 21-Nov-2005 |
| 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 MINOXIDIL
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02356597 | HAIR REGROWTH FORMULA | VITA HEALTH PRODUCTS INC | Solution | MINOXIDIL 20 MG | Marketed |
| 02460181 | HAIR REGROWTH TREATMENT | APOTEX INC | Solution | MINOXIDIL 2 % | Approved |
| 00514500 | LONITEN 10MG | PFIZER CANADA ULC | Tablet | MINOXIDIL 10 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 |
|---|---|---|---|
| 1889 | 2003-09-29 | New Drug Submission (NDS) | MANUFACTURER NAME CHANGE |
| 2436 | 2001-05-30 | New Drug Submission (NDS) | MANUFACTURER NAME CHANGE |
| 3052 | 1998-05-04 | New Drug Submission (NDS) |
International API supply for MINOXIDIL
11 valid EDQM Certificates of Suitability from 11 holders. 10 active FDA Drug Master Files.
Request a quote for LONITEN 2.5MG