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On January 16, 2024, Governor Phil Murphy signed the New Jersey Data Privacy Law, P.L. 2023, c. 266. The law went into effect on January 15, 2025. Please click on this Frequently Asked Questions link to learn more about the new law and your rights under it.
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On January 8, 2024, Governor Murphy signed into law P.L. 2023, c. 237, which, among other things: amended the Contractors’ Business Registration Act (“CBRA,” formerly the “Contractors’ Registration Act”), N.J.S.A. 56:8-136 et seq., and created the “Home Improvement and Home Elevation Contractor Licensing Act,” N.J.S.A. 45:5AAA-1 et seq. For more information on the registration requirements for contractors and businesses under these laws, click here.
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On July 10, 2024, Governor Murphy signed into law the Real Estate Consumer Protection Enhancement Act, P.L. 2024, c.32, which, among other things, requires sellers of residential property located in New Jersey to use the "Seller's Property Condition Disclosure Statement" ("Disclosure Statement," questions 1 through 108).

Additionally, on July 3, 2023, Governor Murphy signed into law P.L. 2023, c.93, which, among other things, requires sellers of all real property located in New Jersey to make certain additional disclosures concerning flood risks on the "Disclosure Statement." On July 15, 2024, the Division published a "Flood Risk Addendum" to the Disclosure Statement (questions 109 through 117), which includes the additional disclosures concerning flood risks.

As a result of these two laws, effective August 1, 2024:
  • Sellers of residential property must complete the Disclosure Statement (questions 1 through 108). A copy of the Disclosure Statement is available here; and
  • All sellers of real property, both residential and non-residential, must complete the Flood Risk Addendum to the Disclosure Statement (questions 109 through 117). A copy of the Flood Risk Addendum is available here.

The Division has created an instruction sheet with additional information regarding the use of these forms. The forms linked above supersede any forms previously posted by the Division, including, but not limited to, the "Amended Disclosure Statement" posted on December 21, 2023.

Press Release


For Immediate Release:
March 1, 2017

Office of The Attorney General
Christopher S. Porrino, Attorney General

Division of Consumer Affairs
Steve C. Lee, Director

Division of Law
Michelle Miller, Acting Director
  For Further Information and Media Inquiries:
Lee Moore, 609-984-4791

New Jersey Joins Multi-State Antitrust Lawsuit Against Six Generic Drug Manufacturing Companies Amended complaint alleges new violations of state antitrust, consumer protection laws


TRENTON -- Attorney General Christopher S. Porrino announced today that New Jersey has joined a multi-state federal lawsuit alleging that six generic drug manufacturing companies conspired to unreasonably restrain trade, artificially inflate and manipulate prices and reduce competition in the U.S. for two generic drugs.

An amended complaint filed today with the U.S. District Court in Connecticut increases from 20 to 40 the number of plaintiff states in the lawsuit, which was initially filed in December 2016.  New Jersey is among the added states. The six defendant companies are Heritage Pharmaceuticals, Inc., Aurobindo Pharma USA, Inc., Citron Pharma, LLC, Mayne Pharma (USA), Inc., Mylan Pharmaceuticals, Inc. and Teva Pharmaceuticals USA, Inc.

The amended complaint adds allegations of state antitrust law violations -- in addition to the federal antitrust claims alleged in the original lawsuit -- and alleges violation of state consumer protection laws in most of the participating states, including New Jersey.

In July 2014, Connecticut authorities launched an investigation into suspicious price increases relative to certain generic pharmaceuticals.  The investigation, which remains ongoing with regard to numerous generic drugs, generic drug companies and key executives, uncovered evidence of a well-coordinated and long-running conspiracy to fix prices and allocate markets for two drugs -- doxycycline hyclate delayed release (an antibiotic) and glyburide (an oral diabetes medication .)

The lawsuit further alleges that the defendants routinely coordinated their schemes through direct interaction with their competitors at industry trade shows, customer conferences and other events, as well as through direct email, phone and text message communications.

This anti-competitive conduct – including efforts to fix and maintain prices, allocate markets and otherwise thwart competition – caused significant, harmful and continuing effects in the country’s healthcare system, the amended complaint alleges.

The multi-state lawsuit announced today was filed under seal with the federal court. Portions of the complaint are redacted in order to avoid compromising the ongoing investigation.

Deputy Attorney General Russell Smith, Deputy Attorney General Jodie Van Wert and Deputy Attorney General Patricia Schiripo, Assistant Section Chief of the Division of Law’s Consumer Fraud Prosecution Section, handled the matter on behalf of the State.

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Last Modified: 3/2/2017 9:33 AM