The full catalog, with the status on every line.
Search 246 APIs. Every line shows its FDA status as of Nov 14, 2026. Every quote includes the lot COA.
Status as of Nov 14, 2026. Sources: FDA 503B categories list (updated Mar 21, 2025), FDA Category 2 page (current Apr 22, 2026), 21 CFR 216.24, 21 CFR 530.41, 21 CFR 600.3(h)(6), HHS FR 2026-22192. No item we list is on the 503B bulks list today. Shortage status is checked when we price your request. Labels are a starting point, not a determination for your facility.
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503B Category 3 (nominated without adequate support).
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FDA named 5-amino-1MQ as ineligible under 503B in a Jan 2026 warning letter.
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503B Category 3 (nominated without adequate support).
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FDA previously listed safety concerns (nomination withdrawn from Category 2).
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503A: covered by the HHS draft six-peptide policy (Oct 30, 2026) in the acetate form, by the listed routes, if all 10 conditions are met. Draft, nonbinding.
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Outside the HHS 503A draft policy (acetate form only).
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Category 1 entry is for ophthalmic use.
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Not found in FDA’s 503B category list; status to be verified.
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503B Category 1 except oral use. Oral human products are on FDA's withdrawn list.
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503B Category 1 except oral use. Oral human products are on FDA's withdrawn list.
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FDA previously listed safety concerns (nomination withdrawn from Category 2).
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Not approved for human use in the US.
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FDA previously listed safety concerns (nomination withdrawn from Category 2).
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FDA previously listed safety concerns (nomination withdrawn from Category 2).
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503B Category 3 (nominated without adequate support).
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503A: covered by the HHS draft six-peptide policy (Oct 30, 2026) in the acetate form, by the listed routes, if all 10 conditions are met. Draft, nonbinding.
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Controlled in some states; flagged by ship-to state.
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Category 1 entry is for ophthalmic solutions.
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Category 2 for injectable and nasal use; Category 1 for other routes.
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503B Category 3 (nominated without adequate support).
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503A: Category 2 (FDA safety risk).
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503B Category 3 (nominated without adequate support).
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503A: covered by the HHS draft six-peptide policy (Oct 30, 2026) in the acetate form, by the listed routes, if all 10 conditions are met. Draft, nonbinding.
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503B Category 3 (nominated without adequate support).
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No current 503B bulk pathway. Off the shortage list (tirzepatide Dec 19, 2024; semaglutide Feb 21, 2025). FDA proposed May 1, 2026 not to add it to the 503B bulks list. Manufacturer must be on FDA Import Alert 66-80 Green List.
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FDA previously listed safety concerns (nomination withdrawn from Category 2).
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FDA previously listed safety concerns (nomination withdrawn from Category 2).
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Not found in FDA’s 503B category list; status to be verified.
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503A: covered by the HHS draft six-peptide policy (Oct 30, 2026) in the acetate form, by the listed routes, if all 10 conditions are met. Draft, nonbinding.
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Outside the HHS 503A draft policy (acetate form only).
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FDA's Jan 20, 2026 warning letter to an outsourcing facility treated NAD+ as ineligible under 503B. The disodium salt trihydrate form is Category 3. Exact form stated on the quote.
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Not found in FDA’s 503B category list; status to be verified.
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FDA previously listed safety concerns (nomination withdrawn from Category 2).
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Outside the HHS 503A draft policy (acetate form only).
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503B Category 3 (nominated without adequate support).
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503B Category 3 (nominated without adequate support).
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503B Category 3 (nominated without adequate support).
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503B Category 3 (nominated without adequate support).
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FDA previously listed safety concerns (nomination withdrawn from Category 2).
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No current 503B bulk pathway. Off the shortage list (tirzepatide Dec 19, 2024; semaglutide Feb 21, 2025). FDA proposed May 1, 2026 not to add it to the 503B bulks list. Manufacturer must be on FDA Import Alert 66-80 Green List. Base form only. FDA says the salt forms have no lawful basis for compounding.
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HHS draft 503A policy lists Semax free base (intranasal), not the acetate.
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Not found in FDA’s 503B category list; status to be verified.
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44 amino acids; biologic status unverified.
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503B Category 3 (nominated without adequate support). Also on the withdrawn-from-Category-2 list.
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Treated as a likely biologic (protein over 40 amino acids); FDA has not ruled on this item.
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503A: covered by the HHS draft six-peptide policy (Oct 30, 2026) in the acetate form, by the listed routes, if all 10 conditions are met. Draft, nonbinding.
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No current 503B bulk pathway. Off the shortage list (tirzepatide Dec 19, 2024; semaglutide Feb 21, 2025). FDA proposed May 1, 2026 not to add it to the 503B bulks list. Manufacturer must be on FDA Import Alert 66-80 Green List.
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503B Category 3 (nominated without adequate support).
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503B Category 3 (nominated without adequate support).
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Not listed? Send the name and spec. We source it and price it on the same sheet. We don't source substances FDA has said can't lawfully be compounded.
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