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Last Updated: March 29, 2024

NAFCILLIN SODIUM Drug Patent Profile


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Which patents cover Nafcillin Sodium, and what generic alternatives are available?

Nafcillin Sodium is a drug marketed by Antibiotice, Apothecon, Eugia Pharma Speclts, Fresenius, Istituto Bio Ita Spa, Sagent Pharms, Sandoz, Steriscience, and Watson Labs Inc. and is included in fifteen NDAs.

The generic ingredient in NAFCILLIN SODIUM is nafcillin sodium. There are eleven drug master file entries for this compound. Ten suppliers are listed for this compound. Additional details are available on the nafcillin sodium profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Nafcillin Sodium

A generic version of NAFCILLIN SODIUM was approved as nafcillin sodium by ISTITUTO BIO ITA SPA on April 20th, 2011.

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Drug patent expirations by year for NAFCILLIN SODIUM
Recent Clinical Trials for NAFCILLIN SODIUM

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SponsorPhase
Federal University of São PauloPhase 4
Fundação de Amparo à Pesquisa do Estado de São PauloPhase 4

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Pharmacology for NAFCILLIN SODIUM
Medical Subject Heading (MeSH) Categories for NAFCILLIN SODIUM

US Patents and Regulatory Information for NAFCILLIN SODIUM

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Watson Labs Inc NAFCILLIN SODIUM nafcillin sodium INJECTABLE;INJECTION 062844-001 Oct 26, 1988 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Watson Labs Inc NAFCILLIN SODIUM nafcillin sodium INJECTABLE;INJECTION 062844-003 Oct 26, 1988 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Watson Labs Inc NAFCILLIN SODIUM nafcillin sodium INJECTABLE;INJECTION 062844-004 Oct 26, 1988 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Antibiotice NAFCILLIN SODIUM nafcillin sodium INJECTABLE;INJECTION 090560-001 Oct 3, 2011 AP RX No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

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