Amobarbital Sodium for Injection
» Amobarbital Sodium for Injection is Amobarbital Sodium suitable for parenteral use.
Constituted solution—
At the time of use, it meets the requirements for Constituted Solutions under Injections 
1
.
1.
Bacterial endotoxins 85—
It contains not more than 0.4 USP Endotoxin Unit per mg of amobarbital sodium.
85—
It contains not more than 0.4 USP Endotoxin Unit per mg of amobarbital sodium.
Loss on drying 731—
Dry about 1 g, accurately weighed, at 105
for 4 hours: it loses not more than 1.0% of its weight.
731—
Dry about 1 g, accurately weighed, at 105 for 4 hours: it loses not more than 1.0% of its weight.
Other requirements—
It conforms to the Definition, responds to the Identification tests, and meets the requirements for Completeness of solution, pH, Heavy metals, and Assay under Amobarbital Sodium. It meets also the requirements for Sterility Tests 71, Uniformity of Dosage Units 905, and Labeling under Injections 1.
71, Uniformity of Dosage Units 905, and Labeling under Injections 1.
Auxiliary Information—
Please check for your question in the FAQs before contacting USP.
| Topic/Question | Contact | Expert Committee |
| Monograph | Ravi Ravichandran, Ph.D.
Senior Scientist 1-301-816-8330 |
(MDPP05) Monograph Development-Psychiatrics and Psychoactives |
| Reference Standards | Lili Wang, Technical Services Scientist 1-301-816-8129 RSTech@usp.org |
|
| 85 |
Radhakrishna S Tirumalai, Ph.D.
Senior Scientist 1-301-816-8339 |
(MSA05) Microbiology and Sterility Assurance |
USP32–NF27 Page 1537