ZTE-105 Formula Gentle Detoxing. Contents 1000 mL
Reason Out-of-specification test results obtained for identification testing based on HPTLC analysis.
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Reason Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Reason Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Reason Subpotent
Reason Presence of Foreign Tablets/Capsules; A single foreign tablet Hydrochlorothiazide/Lisinopril 25/20 was found in one bottle
Reason Labeling: Label error on declared strength - autoinjector devices labeled as 0.75 mg / 0.5 mL actually contain 1.5 mg / 0.5 mL of product.
Reason Lack of Assurance of Sterility
Reason A 500 count bottle of Carvedilol 25 mg tablets contained two Paroxetine Tablets, 40 mg. Product was repackaged into 180 count bottles.
Reason Failed impurities/degradation specification: Out of Specification for an unknown impurity observed in topical product.
Reason Failed Impurities Specifications: Out of Specification impurity results obtained during routine testing.
Reason Presence of Foreign Tablets/Capsules; report of two Paroxetine tablets were found in the bottle
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns
Reason Lack of Assurance of Sterility: FDA inspection raised sterility assurance concerns