US FDA approves Watson ANDA for Oxycodone and Acetaminophen tablets – Pharmaceutical…

US FDA has approved Watson Pharmaceuticals’ abbreviated new drug application (ANDA) for Oxycodone and Acetaminophen tablets, USP 7.5 mg/500 mg and 10 mg/650 mg.

The tablets are the generic equivalent to Endo Pharmaceuticals’ Percocet tablets to treat moderate to moderately severe pain.

The tablet will be manufactured at Watson’s Miami, Florida facility in US.

Headquartered in Corona, US, Watson Pharmaceuticals develops, manufactures and sells proprietary and off-patent pharmaceutical products.

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US FDA approves Watson ANDA for Oxycodone and Acetaminophen tablets – Pharmaceutical…

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