NAD+ Nicotinamide Adenine Dinucleotide, Lyophilized powder for reconstitution, Multi-Dose 500 mg per vial, Each ML contains: 0.288% Sodium Phosphate Monobasic USP, 0.42% Sodium Phosphate Dibasic USP, 5% Mannitol USP, Sterile Water for Injection USP, Rx Only, Olympia Pharmaceuticals 6700 Conroy Rd., Ste. 155, Orlando, FL 32835 NDC: 73198-0083-00
Reported: March 30, 2022 Initiated: March 8, 2022 #D-0719-2022
Product Description
NAD+ Nicotinamide Adenine Dinucleotide, Lyophilized powder for reconstitution, Multi-Dose 500 mg per vial, Each ML contains: 0.288% Sodium Phosphate Monobasic USP, 0.42% Sodium Phosphate Dibasic USP, 5% Mannitol USP, Sterile Water for Injection USP, Rx Only, Olympia Pharmaceuticals 6700 Conroy Rd., Ste. 155, Orlando, FL 32835 NDC: 73198-0083-00
Reason for Recall
Product found to be Sub Potent or Exceeded reconstitution time
Details
- Recalling Firm
- Olympia Compounding Pharmacy dba Olympia Pharmacy
- Units Affected
- 2634 vials
- Distribution
- Nationwide in the USA including Puerto Rico.
- Location
- Orlando, FL
Frequently Asked Questions
What product was recalled? ▼
NAD+ Nicotinamide Adenine Dinucleotide, Lyophilized powder for reconstitution, Multi-Dose 500 mg per vial, Each ML contains: 0.288% Sodium Phosphate Monobasic USP, 0.42% Sodium Phosphate Dibasic USP, 5% Mannitol USP, Sterile Water for Injection USP, Rx Only, Olympia Pharmaceuticals 6700 Conroy Rd., Ste. 155, Orlando, FL 32835 NDC: 73198-0083-00. Recalled by Olympia Compounding Pharmacy dba Olympia Pharmacy. Units affected: 2634 vials.
Why was this product recalled? ▼
Product found to be Sub Potent or Exceeded reconstitution time
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 30, 2022. Severity: Moderate. Recall number: D-0719-2022.
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