Actual Medicinal Product (AMP) -
Humatrope 12mg powder and solvent for solution for injection cartridges (Eli Lilly and Company Ltd)
Name Details
|
Current Name
Humatrope 12mg powder and solvent for solution for injection cartridges
|
Start Date
18-03-2005
|
End Date
|
|
|
Abbreviated Name
Humatrope 12mg inj cartridges
|
Start Date
01-05-2009
|
|
| Humatrope 12mg pdr & solv for soln for inj cartridges |
Previous Start Date
18-03-2005
|
Previous End Date
30-04-2009
|
Summary
- Controlled Drug Category
- Schedule 4 (CD Anab)
- Licensed Route
- Subcutaneous
- Availability Restrictions
- Not available
- Licensing Authority
- Medicines - MHRA/EMA
Codes
| BNF |
|
Previous BNF
06050100
|
Start Date
27-06-2005
|
End Date
03-04-2022
|
SNOMED Codes
|
Code
|
Start Date
|
End Date
|
| 9119411000001101 |
18-03-2005 |
|
Actual Medicinal Product Pack (AMPP) Information