RecallHawk

NORINYL 1+35 21-DAY

ALLERGAN

Summary

FDA approved NORINYL 1+35 21-DAY by ALLERGAN. NDA (New Drug) approval (Labeling) on 2022-04-29. TABLET, ORAL-21.

Details

Source

Drug Approval

External ID

NDA017565-86

Action Date

2022-04-29

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

NORINYL 1+35 21-DAY, TABLET, ORAL-21. Application: NDA017565

Company

Context & Analysis

ALLERGAN has 5 FDA actions in our database.

Frequently Asked Questions

How often does ALLERGAN have FDA actions?

ALLERGAN has 5 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 "NDA017565-86" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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