Last Updated: November 8, 2026

Inforlife Company Profile

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What is the competitive landscape for INFORLIFE

INFORLIFE has eleven approved drugs.

There are four US patents protecting INFORLIFE drugs.

Summary for Inforlife
US Patents:4
Tradenames:11
Ingredients:10
NDAs:11
Patent Litigation for Inforlife: See patent lawsuits for Inforlife

Drugs and US Patents for Inforlife

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Inforlife NOREPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE norepinephrine bitartrate SOLUTION;INTRAVENOUS 215700-004 Oct 15, 2025 RX Yes Yes RE49443 ⤷  Start Trial Y ⤷  Start Trial
Inforlife NOREPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE norepinephrine bitartrate SOLUTION;INTRAVENOUS 215700-001 Sep 15, 2022 RX Yes Yes RE49422 ⤷  Start Trial Y ⤷  Start Trial
Inforlife LEVOFLOXACIN IN DEXTROSE 5% IN PLASTIC CONTAINER levofloxacin INJECTABLE;INJECTION 090343-003 Jul 7, 2011 AP RX No Yes ⤷  Start Trial ⤷  Start Trial
Inforlife ACETAMINOPHEN acetaminophen SOLUTION;INTRAVENOUS 215403-001 May 3, 2023 AP1 RX No No ⤷  Start Trial ⤷  Start Trial
Inforlife NOREPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE norepinephrine bitartrate SOLUTION;INTRAVENOUS 215700-002 Sep 15, 2022 RX Yes Yes RE49422 ⤷  Start Trial Y ⤷  Start Trial
Inforlife FLUCONAZOLE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER fluconazole INJECTABLE;INJECTION 079104-001 Jul 30, 2009 AP RX No Yes ⤷  Start Trial ⤷  Start Trial
Inforlife NICARDIPINE HYDROCHLORIDE IN 0.83% SODIUM CHLORIDE nicardipine hydrochloride INJECTABLE;INTRAVENOUS 203978-002 Apr 17, 2024 AP RX No No ⤷  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

Supplementary Protection Certificates for Inforlife Drugs

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
0206283 C980016 Netherlands ⤷  Start Trial PRODUCT NAME: LEVOFLOXACINE, DESGEWENST IN DE VORM VAN EEN SOLVAAT, IN HET BIJZONDER LEVOFLOXACINE-HEMIHYDRAAT; NAT. REGISTRATION NO/DATE: RVG 21810 - RVG 21812 19971209; FIRST REGISTRATION: GB 13402/0011 - 13402/0013 19970606
0239710 SPC/GB96/051 United Kingdom ⤷  Start Trial PRODUCT NAME: (S)-(-)-1-PROPYL-2',6'-PIPECOLOXYLIDIDE HYDROCHLORIDE MONOHYDRATE (GENERIC NAME: ROPIVACAINE MONOHYDROCHLORIDE MONOHYDRATE); REGISTERED: SE 12319 19950915; SE 12322 19950915; SE 12323 19950915; UK 0017/0375 19960517; UK 0017/0376 19960517; UK 0017/0377 19960517; UK 0017/0378 19960517
0328535 96C0021 Belgium ⤷  Start Trial PRODUCT NAME: LANSOPRAZOLE + CLARITHROMYCINE + METRONIDAZOLE; REGISTRATION NO/DATE IN FRANCE: K 27 17033R DU 19960209; REGISTRATION NO/DATE AT EEC: K 27 17033R DU 19960209
1429780 132013902137451 Italy ⤷  Start Trial PRODUCT NAME: CIPROFLOXACINA E DESAMETASONE(CILODEX); AUTHORISATION NUMBER(S) AND DATE(S): 48976, 20120810;041182015/M, 20121106
0275821 01C0035 France ⤷  Start Trial PRODUCT NAME: ZOLEDRONIC ACID; NAT REG. NO/DATE: EU/1/01/176/001 20010320; FIRST REG.: LI IKS N 55 463 20001128
1429780 13C0012 France ⤷  Start Trial PRODUCT NAME: COMBINAISON DE CIPROFLOXACINE ET DE DEXAMETHASONE, EN PARTICULIER DE CHLORHYDRATE DE CIPROFLOXACINE ET DE DEXAMETHASONE; NAT. REGISTRATION NO/DATE: NL 41308 20121214; FIRST REGISTRATION: 48976 20120808
0206283 98C0041 Belgium ⤷  Start Trial PRODUCT NAME: LEVOFLOXACINUM HEMIHYDRICUM; NAT. REGISTRATION NO/DATE: 354 IS 370 F3 19980624; FIRST REGISTRATION: GB 134020011 19970606
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description
Similar Applicant Names
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