Source: Medicines & Healthcare Products Regulatory Agency (GB) Revision Year: 2019 Publisher: Eli Lilly and Company Limited, Lilly House, Priestley Road, Basingstoke, Hampshire RG24 9NL
Humulin I (Isophane) 100 IU/ml suspension for injection in vial.
| Pharmaceutical Form |
|---|
|
A suspension for injection in a vial. Humulin I is a sterile suspension of a white, crystalline precipitate of isophane human insulin in an isotonic phosphate buffer. |
1 ml contains 100 IU insulin human (produced in E. coli by recombinant DNA technology).
One vial contains 10 ml equivalent to 1000 IU of isophane insulin.
For a full list of excipients, see section 6.1.
| Active Ingredient | Description | |
|---|---|---|
| Insulin (human) |
The blood glucose lowering effect of insulin is due to the facilitated uptake of glucose following binding of insulin to receptors on muscle and fat cells and to the simultaneous inhibition of glucose output from the liver. |
| List of Excipients |
|---|
|
m-cresol The following may be used to adjust pH; hydrochloric acid and/or sodium hydroxide. |
10 ml of suspension in a vial (type I glass) with a stopper (rubber) sealed with a seal (aluminium) combined with a flip top (plastic). Pack size 1 or 2 or 5 (5 × 1). Not all pack sizes may be marketed.
Eli Lilly and Company Limited, Lilly House, Priestley Road, Basingstoke, Hampshire RG24 9NL
PL 00006/0666
30 July 2019
| Drug | Countries | |
|---|---|---|
| HUMULIN | Australia, Brazil, Canada, Cyprus, Germany, Ecuador, Estonia, Finland, Hong Kong, Croatia, Ireland, Israel, Japan, Lithuania, Malta, New Zealand, Poland, Romania, Singapore, Turkey, United Kingdom, United States, South Africa |
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