FDA Lists Tolazamide 500 mg Oral Tablet (ANDA070169)

The FDA’s ANDA070169 filing for Tolazamide 500 mg oral tablets by USL Pharma is marked as discontinued.

The U.S. Food and Drug Administration has recorded an Abbreviated New Drug Application (ANDA) identified as ANDA070169 for a Tolazamide product. The product is an oral tablet containing 500 mg of Tolazamide, assigned product number 001. The sponsor listed is USL Pharma. The filing indicates that the product is not a reference drug, does not use a reference standard, and its marketing status is currently marked as discontinued.

FDA Lists Tolazamide 500 mg Oral Tablet (ANDA070169) – Discontinued

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FDA Lists Tolazamide 500 mg Oral Tablet (ANDA070169) – Discontinued

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FDA Lists Tolazamide 500 mg Oral Tablet (ANDA070169) – Discontinued