RecallHawk

GABAPENTIN

WATSON LABS

Summary

FDA approved GABAPENTIN by WATSON LABS. ANDA (Generic) approval (Labeling) on 2025-03-14. CAPSULE, ORAL.

Details

Source

Drug Approval

External ID

ANDA075485-1

Action Date

2025-03-14

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

GABAPENTIN, CAPSULE, ORAL. Application: ANDA075485

Context & Analysis

WATSON LABS has 30 FDA actions in our database.

Frequently Asked Questions

How often does WATSON LABS have FDA actions?

WATSON LABS has 30 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 "ANDA075485-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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