Selank
FDA approval
Not FDA approvedSelank acetate (TP-7) is not an FDA-approved drug. FDA has evaluated it only as a bulk drug substance nominated for use in compounding, and it is not among the six substances on the 503A Bulks List at 21 CFR 216.23(a).
Sources
- FDA, Certain Bulk Drug Substances for Use in Compounding That May Present Significant Safety Risks (503A and 503B category 2, plus "bulk drug substances nominated but withdrawn"), content current as of April 22, 2026 (U.S. Food and Drug Administration, retrieved 2026-09-16)
- 21 CFR 216.23(a), Bulk drug substances that can be used to compound drug products in accordance with section 503A of the FD&C Act (six substances, no peptides) (Office of the Federal Register, retrieved 2026-09-16)
- FDA, Bulk Drug Substances Used in Compounding Under Section 503A of the FD&C Act (U.S. Food and Drug Administration, retrieved 2026-09-16)
Section 503A
Nominated, then withdrawnAs stated on the cited document, dated .
The nomination was withdrawn by the nominator, so FDA is no longer evaluating it. The substance came off the category it was in; it did not move onto the Bulks List.
Sources
- FDA, Certain Bulk Drug Substances for Use in Compounding That May Present Significant Safety Risks (503A and 503B category 2, plus "bulk drug substances nominated but withdrawn"), content current as of April 22, 2026 (U.S. Food and Drug Administration, retrieved 2026-09-16)
Section 503B
Not nominatedAs stated on the cited document, dated .
The substance appears in none of the categories on that nomination document, as of the document's own date.
Appears in none of the three categories on FDA's section 503B nomination document as of that document's own date.
Sources
- FDA, Bulk Drug Substances Nominated for Use in Compounding Under Section 503B of the FD&C Act, updated March 21, 2025 (U.S. Food and Drug Administration, retrieved 2026-09-16)
Verified against FDA's bulk substances page on .