PENTOTHAL READY TO MIX SYRINGE 250MG DIN 00372536
Health Canada record
| Active ingredient(s) | THIOPENTAL SODIUM 250 MG |
|---|---|
| Dosage form | Powder For Solution |
| Route | Intravenous |
| Schedule | CONTROLLED DRUGS (CDSA IV) |
| Class | Human |
| ATC | N01AF03 THIOPENTAL |
| Original market date | 31-Dec-1986 |
| Current status date | 06-Aug-2019 |
| Source | Health Canada DPD |
Establishment licence of the holder
Hospira Healthcare India Pvt. Ltd. — licence , not currently licensed, last inspection rating NC (2017-07-10).
No Canadian shortage report is currently matched to this DIN.
Other Canadian products containing THIOPENTAL SODIUM
| DIN | Product | Company | Form | Strength | Status |
|---|---|---|---|---|---|
| 02145685 | INDUTHOL - PWR IV 93.5G/100G | MTC PHARMACEUTICALS | Powder | THIOPENTAL SODIUM 93.5 G | Cancelled Post Market |
| 00551961 | INTRAVAL SODIUM INJ | MAY & BAKER CANADA INC. | Liquid | THIOPENTAL SODIUM 100 % | Cancelled Post Market |
| 00695017 | PENTOTHAL INJ 25MG/ML | HOSPIRA HEALTHCARE ULC | Powder For Solution | THIOPENTAL SODIUM 25 MG | Cancelled Post Market |
| 00038393 | PENTOTHAL INJ 500MG/SYR | HOSPIRA HEALTHCARE ULC | Powder For Solution | THIOPENTAL SODIUM 500 MG | Cancelled Post Market |
| 00038407 | PENTOTHAL SODIUM INJ 1GM STERILE | HOSPIRA HEALTHCARE ULC | Powder For Solution | THIOPENTAL SODIUM 1 G | Cancelled Post Market |
| 00038415 | PENTOTHAL SODIUM PWS 5GM | HOSPIRA HEALTHCARE ULC | Powder For Solution | THIOPENTAL SODIUM 5 G | Cancelled Post Market |
| 02243344 | THIOTAL 1G | VETOQUINOL N A INC | Powder For Solution | THIOPENTAL SODIUM 1 G | Cancelled Post Market |
| 02060000 | THIOTAL 5G | VETOQUINOL N A INC | Kit; Powder For Solution | THIOPENTAL SODIUM 5 G; WATER 200 ML | Cancelled Post Market |
International API supply for THIOPENTAL SODIUM
0 active FDA Drug Master Files.
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