Details for New Drug Application (NDA): 202138

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NDA 202138 describes KEMEYA, which is a drug marketed by Sun Pharm and is included in one NDA. Additional details are available on the KEMEYA profile page.

The generic ingredient in KEMEYA is drospirenone; ethinyl estradiol. There are eleven drug master file entries for this compound. Sixteen suppliers are listed for this compound. Additional details are available on the drospirenone; ethinyl estradiol profile page.

Summary for 202138

Tradename:	KEMEYA
Applicant:	Sun Pharm
Ingredient:	drospirenone; ethinyl estradiol
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL-28			Strength	3MG;0.03MG
Approval Date:	Mar 13, 2019	TE:		RLD:	No

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