Last Updated: November 13, 2026

Millicent Mfg Pr Company Profile

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What is the competitive landscape for MILLICENT MFG PR

MILLICENT MFG PR has two approved drugs.

There is one US patent protecting MILLICENT MFG PR drugs.

Summary for Millicent Mfg Pr
US Patents:1
Tradenames:2
Ingredients:2
NDAs:2

Drugs and US Patents for Millicent Mfg Pr

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Millicent Mfg Pr FEMRING estradiol acetate INSERT, EXTENDED RELEASE;VAGINAL 021367-001 Mar 20, 2003 RX Yes No ⤷  Start Trial ⤷  Start Trial
Millicent Mfg Pr FEMLYV ethinyl estradiol; norethindrone acetate TABLET, ORALLY DISINTEGRATING;ORAL 218718-001 Jul 22, 2024 RX Yes Yes ⤷  Start Trial ⤷  Start Trial
Millicent Mfg Pr FEMLYV ethinyl estradiol; norethindrone acetate TABLET, ORALLY DISINTEGRATING;ORAL 218718-001 Jul 22, 2024 RX Yes Yes 12,178,824 ⤷  Start Trial Y ⤷  Start Trial
Millicent Mfg Pr FEMRING estradiol acetate INSERT, EXTENDED RELEASE;VAGINAL 021367-002 Mar 20, 2003 RX Yes Yes ⤷  Start Trial ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Expired US Patents for Millicent Mfg Pr

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Millicent Mfg Pr FEMRING estradiol acetate INSERT, EXTENDED RELEASE;VAGINAL 021367-001 Mar 20, 2003 5,855,906 ⤷  Start Trial
Millicent Mfg Pr FEMRING estradiol acetate INSERT, EXTENDED RELEASE;VAGINAL 021367-002 Mar 20, 2003 5,855,906 ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration

Supplementary Protection Certificates for Millicent Mfg Pr Drugs

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
1453521 132016000025143 Italy ⤷  Start Trial PRODUCT NAME: LEVONORGESTREL ED ETINILESTRADIOLO(SEASONIQUE); AUTHORISATION NUMBER(S) AND DATE(S): 17/0017/15-S, 20150211;042139016, 20150414
2782584 2021C/558 Belgium ⤷  Start Trial PRODUCT NAME: COMPOSITION CONTENANT A LA FOIS DE L'ESTRADIOL (17--ESTRADIOL), EVENTUELLEMENT SOUS FORME D'UN SEL, HYDRATE OU SOLVATE PHARMACEUTIQUEMENT ACCEPTABLE DE CELUI-CI (Y COMPRIS SOUS FORME HEMIHYDRATEE), ET DE LA PROGESTERONE; AUTHORISATION NUMBER AND DATE: BE582231 20210406
1214076 SZ 49/2008 Austria ⤷  Start Trial PRODUCT NAME: WIRKSTOFFKOMBINATION VON ETHINYLESTRADIOL UND DROSPIRENON
0771217 07C0001 France ⤷  Start Trial PRODUCT NAME: ETHINYLESTRADIOL BETADEX CLATHRATE; NAT. REGISTRATION NO/DATE: NL 32343 20060710; FIRST REGISTRATION: NL - RVG 31781 20050804
1380301 CA 2009 00017 Denmark ⤷  Start Trial PRODUCT NAME: ETHINYLESTRADIOL (SOM BETADEXCLATHRAT) OG DROSPIRENON; NAT. REG. NO/DATE: 42417 (DK) 20080619; FIRST REG. NO/DATE: NL 33842 20070629
1453521 122015000093 Germany ⤷  Start Trial PRODUCT NAME: LEVONORGESTREL UND ETHINYLESTRADIOL; NAT. REGISTRATION NO/DATE: 87675.00.00 20150720; FIRST REGISTRATION: SLOWAKEI 17/0017/15-S 20150129
1214076 C01214076/01 Switzerland ⤷  Start Trial PRODUCT NAME: DROSPIRENONE + ETHINYLESTRADIOL; REGISTRATION NUMBER/DATE: SWISSMEDIC 57946 13.06.2008
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description
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