RecallHawk

OXYCODONE AND ACETAMINOPHEN

WES PHARMA INC

Summary

FDA approved OXYCODONE AND ACETAMINOPHEN by WES PHARMA INC. ANDA (Generic) approval (REMS) on 2026-06-18. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA207510-15

Action Date

2026-06-18

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

OXYCODONE AND ACETAMINOPHEN, TABLET, ORAL. Application: ANDA207510

Context & Analysis

WES PHARMA INC has 2 FDA actions in our database.

Frequently Asked Questions

How often does WES PHARMA INC have FDA actions?

WES PHARMA INC has 2 FDA actions in our database, including 0 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "ANDA207510-15" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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