Is Evofem, Inc. FDA approved?

Evofem, Inc. holds no registered establishment of its own; 3 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.

What drugs does Evofem, Inc. make?

3 products are listed under Evofem, Inc. in the openFDA NDC Directory, most often as gel; granule. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Evofem, Inc.

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 0
Active NDC listings: 3
Labeller names: 2
Live patents: 15
Exclusivities: 1
Countries: 0

Catalogue

Drug listings by form and route

3 active NDC listings: 3 human prescription drug. By marketing category: NDA 3.

Dosage form	NDCs
gel	2
granule	1

Route	NDCs
vaginal	2
oral	1

Labeller name on the listing	NDCs
evofem, inc.	2
evofem inc.	1

Exclusivity

Patents and exclusivities

Patent	Product	Covers	Expiry
10568855	PHEXXcitric acid; lactic acid; potassium bitartrate	use	Mar 2033
11337989	PHEXXcitric acid; lactic acid; potassium bitartrate	use	Mar 2033
11439610	PHEXXcitric acid; lactic acid; potassium bitartrate	substance, product	Mar 2033
11992472	PHEXXcitric acid; lactic acid; potassium bitartrate	use	Mar 2033
10335390	SOLOSECsecnidazole	product	Sept 2035
10682338	SOLOSECsecnidazole	product	Sept 2035
10849884	SOLOSECsecnidazole	product	Sept 2035
10857133	SOLOSECsecnidazole	product	Sept 2035
11000507	SOLOSECsecnidazole	product	Sept 2035
11000508	SOLOSECsecnidazole	product	Sept 2035
11020377	SOLOSECsecnidazole	product	Sept 2035
11324721	SOLOSECsecnidazole	product	Sept 2035
11602522	SOLOSECsecnidazole	product	Sept 2035
11684607	SOLOSECsecnidazole	product	Sept 2035
12280037	SOLOSECsecnidazole	use	Dec 2041

Product	Exclusivity	Until
SOLOSECSECNIDAZOLE	GAIN Qualified infectious disease product (GAIN)	Sept 2027

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
Phexx	lactic acid, L-, citric acid monohydrate, and potassium bitartrate	gel, vaginal	69751-101NDA
Phexxi	lactic acid, L-, citric acid monohydrate, and potassium bitartrate	gel, vaginal	69751-100NDA
Solosec	secnidazole	granule, oral	69751-400NDA

Enquiry

Common questions

Is Evofem, Inc. FDA approved?: Evofem, Inc. holds no registered establishment of its own; 3 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does Evofem, Inc. make?: 3 products are listed under Evofem, Inc. in the openFDA NDC Directory, most often as gel; granule. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.