Master formulation and compounding records

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Ingredients

Ingredient chips: FDA 503A categories and lists, 21 CFR 216.24, and NIOSH hazardous drugs. Check an ingredient in detail, including FDA shortages.

Equipment
Compounding steps
Quality control

Beyond-use date

Current: 10 days · Duration supported by the cited stability study for this formula, container, and storage.

Work out the BUD
Preparation
Dosage form
Storage

Beyond-use date

14 days

Refrigerator

  • Nonpreserved aqueous dosage form: 14 days, refrigerated.

USP <795> §10.4 (CNSPs requiring shorter BUDs), Table 4 (BUD limits by type of preparation)

Rules current as of the USP <795> and <797> revisions official November 1, 2023. Verify against the current official USP chapter before assigning a BUD.

References

Master formulation record: Oseltamivir oral solution 15 mg/mL

Oral solution · Oral · Nonsterile (USP <795>) · Batch 100 mL

Ingredients

IngredientRoleQuantity
Oseltamivir (as phosphate)active1.5 g
Sodium benzoatepreservative
Purified watervehicle q.s.

Equipment

  • Class A prescription balance or electronic balance
  • Mortar and pestle
  • Graduated cylinder

Quality control

  • Visual inspection: uniform appearance, no foreign matter
  • Final volume or weight checked

Packaging, storage, and BUD

Container: Type II amber glass bottles (125 mL), filled to allow for expansion on freezing · Storage: Refrigerator · BUD: 10 days

Basis: Duration supported by the cited stability study for this formula, container, and storage. Ramirez JCR et al. Pharmaceutics. 2026;18(9):1130. PMC13610113

Labeling

Shake well. Store as directed. Discard after the beyond-use date.

References

  1. Ramirez JCR, Sáez AG, Madrid MEM, Viney AC, Herreros JMA, Rojo PA. Stability Study of a Frozen Oseltamivir 15 mg/mL Oral Solution in Amber Glass Bottles. Pharmaceutics. 2026;18(9):1130. PMC13610113. https://pmc.ncbi.nlm.nih.gov/articles/PMC13610113/

Notes

Stored frozen up to 75 days, then refrigerated up to 10 days after thawing.

Prepared by
Approved by
Date

Record contents follow the master formulation and compounding record sections of USP <795> and <797>; check your state board's requirements. For licensed clinicians. Use with clinical judgment.