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Name | Diamorphine hydrochloride powder |
BNF code | 0407020K0AAFPFP |
Date identifier became valid | 26 May 2021 |
Previous product identifier | 348125006 |
Basis of preferred name | BANM - British Approved Name (Modified) |
Date of name applicability | 7 Dec 2004 |
Previous name | Diamorphine hydrochloride |
Basis of previous name | BANM - British Approved Name (Modified) |
Reason for name change | Other |
Prescribing status | Valid as a prescribable product |
Sugar free | ✗ |
Gluten free | ✗ |
Preservative free | ✗ |
CFC free | ✗ |
Non-availability | Actual Products Available |
Non-availability status date | 22 Jul 2019 |
Dose form | Continuous |
Virtual Product Ingredient | |
---|---|
Ingredient | Diamorphine hydrochloride |
Basis of pharmaceutical strength | Based on Ingredient Substance |
Strength value numerator | 1.000 |
Strength value numerator unit | mg |
Strength value denominator | 1.000 |
Strength value denominator unit | mg |
Dose Form | |
Formulation | Not applicable |
Drug Route | |
Route | Route of administration not applicable |
Controlled Drug Prescribing Information | |
Controlled Drug category | Schedule 2 (CD) |
Actual Medicinal Products | |
Diamorphine hydrochloride powder (Special Order) | |
Virtual Medicinal Product Packs | |
Diamorphine hydrochloride powder 10 gram | |
Diamorphine hydrochloride powder 1 gram | |
Diamorphine hydrochloride powder 25 gram | |
Diamorphine hydrochloride powder 2 gram | |
Diamorphine hydrochloride powder 5 gram |
dm+d data retrieved from TRUD: release NHSBSA_3.1.0_20250310000001, imported on 11th March 2025 at 03:57:45.