RecallHawk

BALZIVA (NORETHINDRONE AND ETHINYL ESTRADIOL)

BARR

Summary

FDA approved BALZIVA (NORETHINDRONE AND ETHINYL ESTRADIOL) by BARR. ANDA (Generic) approval (Labeling) on 2022-04-29. TABLET, ORAL-28.

Details

Source

Drug Approval

External ID

ANDA076238-25

Action Date

2022-04-29

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

BALZIVA (generic: NORETHINDRONE AND ETHINYL ESTRADIOL), TABLET, ORAL-28. Application: ANDA076238

Company

Context & Analysis

BARR has 16 FDA actions in our database.

Frequently Asked Questions

How often does BARR have FDA actions?

BARR has 16 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 "ANDA076238-25" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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