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A diagnostic-use formulation (0.05 mg base per ampule, for evaluating the pituitary's capacity to secrete growth hormone) was approved December 28, 1990 under NDA 19-863

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The FDA specifically warned about peptide-related impurities and API characterization problems in other words, that whats in the vial might not be 100% pure BPC-157, and even if it is, the peptide could degrade or contain variants

Medical professionals are trained to handle such situations and can provide the necessary assistance or alternatives

Adding bacteriostatic water or sterile saline creates a workable liquid concentration measured in micrograms per graduation mark on laboratory syringes