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Beyond Use Dating For Sterile Compounding

Beyond use dates (BUDs) define the maximum time periods that compounded sterile preparations (CSPs) may be stored or transported, in contrast to expiration dates set by manufacturers. BUDs depend on a CSP's stability and sterility, and are limited by USP Chapter 797 to periods ranging from 1 hour to 45 days based on risk level. If a BUD exceeds these limits, a sterility test is required regardless of quantity compounded. Single dose containers have shorter BUDs than multi-dose containers or pharmacy bulk packages.

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2K views2 pages

Beyond Use Dating For Sterile Compounding

Beyond use dates (BUDs) define the maximum time periods that compounded sterile preparations (CSPs) may be stored or transported, in contrast to expiration dates set by manufacturers. BUDs depend on a CSP's stability and sterility, and are limited by USP Chapter 797 to periods ranging from 1 hour to 45 days based on risk level. If a BUD exceeds these limits, a sterility test is required regardless of quantity compounded. Single dose containers have shorter BUDs than multi-dose containers or pharmacy bulk packages.

Uploaded by

Arum Winda Setyorini
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BEYOND USE DATING FOR STERILE COMPOUNDING

Beyond Use Date (BUD) is very different from expiration date. USP Chapter 797 defines BUD
as the date or time after which a compounded sterile preparation (CSP) may not be stored or
transported and is calculated from the date or time of compounding. Expiration date is a
manufacturer defined term based on very specific testing used for commercially available
products. A CSP cannot be labeled with the term expiration date or any variance thereof. It
must be labeled with a different phrase such as, do not use after or use before etc.

BUDs for CSPs depend on the stability of the compound and the sterility of the compound.
Stability information may be found in literature (such as Trissels Stability of Compounded
Formulations) or may be determined by performing a stability test on the CSP. A point in time
potency test is not equivalent to a stability test. When determining BUDs the stability or the
sterility may be the limiting factor.

If stable and in the absence of sterility testing, USP 797 limits BUDs of CSPs to the following,
based on risk level:

Risk Level Controlled Room Cold Temperature Frozen


Temperature
Immediate Use 1 hour from start of NA NA
compounding
Low Segregated 12 hours or less from NA NA
Compounding Area compounding
Low 48 hours 14 days 45 days
Medium 30 hours 9 days 45 days
High 24 hours 3 days 45 days

If the BUD is extended beyond the allowances by USP Chapter 797, a sterility test that complies
with USP Chapter 71 must be performed regardless of the quantity compounded. For example,
if a high risk sterile eye drop is compounded and a 14 day room temperature BUD is given,
enough extra of the eye drop must be compounded to send for sterility testing.

Single Dose Containers (SDC) and Multiple Dose Containers (MDC)


SDC vial, bag, bottle, syringe Outside ISO 5 environment one hour from
time of puncture or opening
SDC vial , bag, bottle, syringe Inside ISO 5 environment up to 6 hours from
time of puncture or opening
SDC ampule Cannot be stored, any not used must be
discarded immediately
MDC Up to 28 days from time of puncture or
opening unless otherwise specified by
manufacturer
Pharmacy Bulk Package (PBP)
PBP is treated the same as SDC for vials, bags, bottles and syringes in that if opened outside an
ISO 5 environment, the PBP can be used for 1 hour from the time of puncture/opening and if
opened inside an ISO 5 environment, the PBP can be used for up to 6 hours from the time of
puncture/opening. The entire contents of a PBP can be used to compound multiple medium risk
CSPs which may be stored up to 9 days refrigerated or 45 days frozen.

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