ACYCLOVIR SODIUM INJECTION DIN 02239743
Status: Cancelled Pre Market
Holder: IVAX PHARMACEUTICALS INCORPORATED
Molecule: ACYCLOVIR (ACYCLOVIR SODIUM)
Health Canada record
| Active ingredient(s) | ACYCLOVIR (ACYCLOVIR SODIUM) 25 MG |
|---|---|
| Dosage form | Solution |
| Route | Intravenous |
| Schedule | PRESCRIPTION |
| Class | Human |
| ATC | J05AB01 ACYCLOVIR |
| Original market date | |
| Current status date | 16-Oct-2015 |
| Source | Health Canada DPD |
Establishment licence of the holder
Ivax Pharmaceuticals UK — licence , not currently licensed, last inspection rating C (2014-09-13).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing ACYCLOVIR (ACYCLOVIR SODIUM)
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02531224 | ACYCLOVIR SODIUM INJECTION | EUGIA PHARMA INC. | Solution | ACYCLOVIR (ACYCLOVIR SODIUM) 50 MG | Marketed |
| 02494558 | ACYCLOVIR SODIUM INJECTION | AURO PHARMA INC | Solution | ACYCLOVIR (ACYCLOVIR SODIUM) 50 MG | Marketed |
| 02236926 | ACYCLOVIR SODIUM INJECTION | FRESENIUS KABI CANADA LTD | Solution | ACYCLOVIR (ACYCLOVIR SODIUM) 50 MG | Marketed |
| 02231356 | ACYCLOVIR SODIUM FOR INJECTION | ABBOTT LABORATORIES, LIMITED | Powder For Solution | ACYCLOVIR (ACYCLOVIR SODIUM) 500 MG | Cancelled Post Market |
| 02231357 | ACYCLOVIR SODIUM FOR INJECTION | ABBOTT LABORATORIES, LIMITED | Powder For Solution | ACYCLOVIR (ACYCLOVIR SODIUM) 1 G | Cancelled Post Market |
| 02231190 | ACYCLOVIR SODIUM FOR INJECTION | NOVOPHARM LIMITED | Powder For Solution | ACYCLOVIR (ACYCLOVIR SODIUM) 500 MG | Cancelled Post Market |
| 02231191 | ACYCLOVIR SODIUM FOR INJECTION | NOVOPHARM LIMITED | Powder For Solution | ACYCLOVIR (ACYCLOVIR SODIUM) 1 G | Cancelled Post Market |
| 02236916 | ACYCLOVIR SODIUM INJECTION | PFIZER CANADA ULC | Solution | ACYCLOVIR (ACYCLOVIR SODIUM) 25 MG | Cancelled Post Market |
| 02456524 | ACYCLOVIR SODIUM INJECTION | STERIMAX INC | Solution | ACYCLOVIR (ACYCLOVIR SODIUM) 50 MG | Dormant |
| 00605336 | ZOVIRAX | GLAXOSMITHKLINE INC | Powder For Solution | ACYCLOVIR (ACYCLOVIR SODIUM) 500 MG | Cancelled Post Market |
| 00899321 | ZOVIRAX | GLAXOSMITHKLINE INC | Powder For Solution | ACYCLOVIR (ACYCLOVIR SODIUM) 1 G | Cancelled Post Market |
Notices of Compliance
| NOC | Date | Submission | Reason |
|---|---|---|---|
| 192 | 2002-11-20 | Abbreviated New Drug Submission (ANDS) | MANUFACTURER NAME CHANGE |
| 1585 | 1999-03-04 | Abbreviated New Drug Submission (ANDS) |