Actual Medicinal Product (AMP) - Humatrope 1.3mg powder and solvent for solution for injection vials (Eli Lilly and Company Ltd)

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Name Details

Name Start Date End Date
Name Current Name Humatrope 1.3mg powder and solvent for solution for injection vials Start Date 14-06-2004 End Date
Previous Name Previous Name Humatrope 1.3mg injection vials and diluent Start Date 01-10-2003 End Date 13-06-2004
Abbreviated Name Abbreviated Name Humatrope 1.3mg inj vials Start Date 01-05-2009
Previous Abbreviated Name Humatrope 1.3mg pdr & solv for soln for inj vials Previous Start Date 14-09-2004 Previous End Date 30-04-2009

Summary

Discontinued
Controlled Drug Category
Schedule 4 (CD Anab)
Licensed Route
Subcutaneous
Availability Restrictions
Not available
Licensing Authority
Medicines - MHRA/EMA

Codes

BNF Start Date End Date
Previous BNF 06050100 Start Date 27-06-2005 End Date 03-04-2022
SNOMED Codes
Code Start Date End Date
4962411000001109 01-10-2003

Parent Products

Actual Medicinal Product Pack (AMPP) Information

Pack Size Indicative Price Discontinued
1 vial