Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Terminated Initiated Apr 4, 2022 (5 years ago)

NAD+ Nicotinamide Adenine Dinucleotide Lyophilized powder for reconstitution

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failed Reconstitution time

Cause type: Other

Recalls whose stated reason does not fall into the categories above. See the recall's own reason text for the specifics. All other recalls.

What was recalled

NAD+ Nicotinamide Adenine Dinucleotide Lyophilized powder for reconstitution, Multi-Dose 500 mg Per Vial, Rx Only, Olympia Pharmaceuticals 6700 Conroy Rd., Ste. 155, Orlando, FL 32835. NDC 73198-0083-00

Affected NDC 73198-0083-00

Compare with the code on your package — it is the most precise check available.

Drug: Adenine

Recalling firm
Olympia Compounding Pharmacy dba Olympia Pharmacy
NDC code
73198-0083-00
Origin
FL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0828-2022 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other Adenine recalls

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Other recalls by Olympia Compounding Pharmacy dba Olympia Pharmacy

All 2022 recalls