SRONYX (LEVONORGESTREL AND ETHINYL ESTRADIOL)
Summary
FDA approved SRONYX (LEVONORGESTREL AND ETHINYL ESTRADIOL) by DR REDDYS LABS SA. ANDA (Generic) approval (Labeling) on 2022-04-29. TABLET, ORAL-28.
Details
Source
Drug Approval
External ID
ANDA077681-15
Action Date
2022-04-29
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
SRONYX (generic: LEVONORGESTREL AND ETHINYL ESTRADIOL), TABLET, ORAL-28. Application: ANDA077681
Company
Context & Analysis
DR REDDYS LABS SA has 14 FDA actions in our database.
Frequently Asked Questions
How often does DR REDDYS LABS SA have FDA actions?
DR REDDYS LABS SA has 14 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 "ANDA077681-15" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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