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HALOETTE (ETHINYL ESTRADIOL; ETONOGESTREL) — FDA Approval ANDA211328 (DR REDDYS LABS SA)

HALOETTE (ETHINYL ESTRADIOL; ETONOGESTREL) — FDA Approval ANDA211328 (DR REDDYS LABS SA) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: HALOETTE; Active ingredients: ETHINYL ESTRADIOL; ETONOGESTREL; Application number: ANDA211328.

Brand nameHALOETTE
Active ingredientsETHINYL ESTRADIOL; ETONOGESTREL
Application numberANDA211328
SponsorDR REDDYS LABS SA
Dosage formRING
RouteVAGINAL
Marketing statusPrescription
Products in application1
First approval date20220805
SourceopenFDA Drugs@FDA

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