RecallHawk

NORGESTIMATE AND ETHINYL ESTRADIOL

GLENMARK SPECLT

Summary

FDA approved NORGESTIMATE AND ETHINYL ESTRADIOL by GLENMARK SPECLT. ANDA (Generic) approval (Labeling) on 2022-04-29. TABLET, ORAL-28.

Details

Source

Drug Approval

External ID

ANDA204057-5

Action Date

2022-04-29

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

NORGESTIMATE AND ETHINYL ESTRADIOL, TABLET, ORAL-28. Application: ANDA204057

Context & Analysis

GLENMARK SPECLT has 8 FDA actions in our database.

Frequently Asked Questions

How often does GLENMARK SPECLT have FDA actions?

GLENMARK SPECLT has 8 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 "ANDA204057-5" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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