Sotalol hydrochloride 5 mg/mL oral suspension
CGR-NZ-003 · New Zealand Compounding Working Group — NZ standardised oral formulation batch sheet; hosted by PSNZ
WORKSHEET FOR LOCAL APPROVAL — source authority does not replace batch approval.
Source formula
| Ingredient | Source quantity |
|---|---|
| Sotalol hydrochloride 80 mg tablets (Mylan) | 5 δισκία / tablets |
| Ora-Blend (selected source option) | q.s. ad 80 mL |
Quantities refer to the source batch. This website does not automatically scale formulas, assign doses or calculate BUD.
Description
Documented in sourcePinkish-white suspension.
References: [1]
Use and action
Documented in sourceAntiarrhythmic with beta blockade; QT-prolongation risk and monitoring requirements at initiation/reinitiation.
Active-drug context from another product’s labelling; it does not establish stability or dosing of this compounded preparation.
References: [2]
Specifications
Documented in sourceCheck yield and appearance. No analytical test limits given. Source appearance: pinkish white.
References: [1]
Light
Not establishedNo specific information is established by the consulted sources. Complete this before local approval where critical to this preparation.
References: [1]
Air
Not establishedNo specific information is established by the consulted sources. Complete this before local approval where critical to this preparation.
References: [1]
Water and solubility
Not establishedNo specific information is established by the consulted sources. Complete this before local approval where critical to this preparation.
References: [1]
Humidity
Not establishedNo specific information is established by the consulted sources. Complete this before local approval where critical to this preparation.
References: [1]
Temperature
Partial evidenceFor the finished product the source specifies:
Amber plastic bottle. Prefer 2–8 °C; room temperature ≤25 °C is allowed. Shake well.
References: [1]
pH and related incompatibilities
Not establishedNo specific information is established by the consulted sources. Complete this before local approval where critical to this preparation.
References: [1]
Other incompatibilities
Not establishedNo specific information is established by the consulted sources. Complete this before local approval where critical to this preparation.
References: [1]
Ingredient-specific information
Not establishedNo specific information is established by the consulted sources. Complete this before local approval where critical to this preparation.
References: [1]
Personal protective equipment
Partial evidenceComplete formula-specific PPE is not specified. Select gloves, eye protection and exposure controls using the exact materials’ SDS and the local risk assessment.
Supplementary AEMPS framework: clean long-sleeved laboratory clothing, hair covering and dedicated footwear/overshoes. Powder handling requires suitable eye/respiratory protection; change gloves with activity or damage. Select the exact type/material using SDS and risk assessment.
Risks and precautions
Partial evidenceA complete formula-specific hazard classification is not established. Assess potency, dust/aerosol, allergens, solvents, microbial risk and cross-contamination using the actual materials and process. Absence of a flag does not establish absence of hazard.
References: [1]
Compounding conditions
Partial evidenceFollow the addition sequence, temperatures and times stated under Preparation Procedure. The specific monograph is not a complete qualification of the local facility/equipment.
References: [1]
BUD rationale
Documented in sourceSource period: 30 days under the permitted storage conditions.
The source period applies to its exact composition, method and packaging. It is not this batch’s expiry date and cannot be transferred to another vehicle/strength. Calculate the actual date in the blank batch record.
References: [1]
Bases and dependencies
Partial evidenceNo separate base is identified in the dependency register. Check any commercial vehicles/compound excipients listed in the formula.
References: [1]
Equipment
Editorial checklistIndicative checklist derived from the method: Balance of suitable resolution, Containers and mixing tools compatible with the materials, Capsule-filling equipment. Selection/qualification is defined locally.
References: [1]
Preparation procedure
Documented in sourcePulverise tablets or capsule contents. Levigate with a little of the specified vehicle, dilute progressively, transfer quantitatively with rinses, make to final volume and mix.
References: [1]
Observations
Documented in sourceOra-Blend option reproduced. Source also permits premixed Ora-Plus/Ora-Sweet 1:1 and SF variants. Record one vehicle choice before compounding; these are alternatives, not cumulative ingredients.
References: [1]
Packaging
Documented in sourceAmber plastic bottle as specified by the sheet.
References: [1]
Quality control
Partial evidenceCheck yield and appearance. No analytical test limits given. Source appearance: pinkish white.
References: [1]
Storage
Documented in sourceAmber plastic bottle. Prefer 2–8 °C; room temperature ≤25 °C is allowed. Shake well.
References: [1]
Dispensing and directions
Partial evidenceNo additional special directions are established beyond the source route, storage and notes. Complete patient details, dose and directions from the prescription.
References: [1]
Labelling
editorial_specimenSotalol hydrochloride 5 mg/mL oral suspension
Strength/variant: __________ Quantity: __________
Batch: __________ Prepared: __________ Use by: __________
Από του στόματος / Oral use
Dose/directions: __________
Storage: Amber plastic bottle. Prefer 2–8 °C; room temperature ≤25 °C is allowed. Shake well.
Shake before use.
References: [1]
Sources and traceability
- New Zealand Compounding Working Group — NZ standardised oral formulation batch sheet; hosted by PSNZ
1.0 / 04/09/2025 · PDF pp. 1–2 · B1
Review date reported in supplied metadata: 2026-09-10
- DailyMed / NLM: SOTALOL HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS]
SPL published Aug 31, 2026 · Indications / warnings / pharmacology · C1 context only
Review date reported in supplied metadata: 2026-09-10
- PN/L/PG/002/00 INDUMENTARIA
Διαθέσιμο κείμενο / Retrieved text · PDF pp. 1–5 · A1
Review date reported in supplied metadata: 2026-09-10
Provenance and reuse
This record comes from the supplied v4 collection. Primary-source rights and licences remain separate. No new comprehensive licence review has been performed for the earlier 239 records.
SHA-256 of the supplied PDF: 0ec5be54ced1f9269f1baaf53f5021d48218bb825035964cafab0ad788338f47