Skip to main content
All lobbying filings

Astrazeneca Pharmaceuticals LP

Astrazeneca Pharmaceuticals LP filed a Q2 report for Astrazeneca Pharmaceuticals LP on July 21, 2025.

Lobbying for Astrazeneca Pharmaceuticals LP

As filed: ASTRAZENECA PHARMACEUTICALS LP for ASTRAZENECA PHARMACEUTICALS LP.

All filings by Astrazeneca Pharmaceuticals LP · Everything Astrazeneca Pharmaceuticals LP has reported

 Filing · LD-2 quarterly report Q2 report
Reporting period
2nd Quarter 2025
Apr 1 - June 30 · Posted Jul 21, 2025
Expenses
$1,840,000
What this organization spent lobbying with its own staff. Reported using the LDA's own definitions (method A): the three LDA methods count different costs, so an expenses figure is not comparable across filers that used different ones.
Client based in
Delaware

Official filing document

 Government bodies contacted 6

The chambers, agencies and offices the filer named. It does not say who inside them was contacted, or when. Each name opens every filing that named the same body.

 Lobbying activity 6

HR 1, One Big Beautiful Bill Act HR 946/S 1862, Optimizing Research Progress Hope and New Cures (ORPHAN Cures) Act HR 1262/ S 932, Give Kids A Chance Act HR 1503/S 2916, Prescription Information Modernization Act Implementation of the Inflation Reduction Act (IRA) -- with specific focus on drug negotiation (orphan drug exemption language); consideration of small molecule drugs, biologics, and genetically targeted technologies; duplicate discounts as required by IRA; Policies related to the definition of a qualifying single source drug under the IRA; Issues related to the IRA definition of a drug for purposes of price negotiation selection; Issues related to expanding/amending the orphan drug exclusion in IRA Orphan drugs and diseases Education to Hill staff on next generation propellant and PFAS Issues related to pharmacy benefit manager (PBM) reform; Policies related to 340B rebate model for IRA compliance; Reforms to the 340B program; Issues related to mitigation of 340B Issues related to the price and manufacture of inhaled medicines Issues related to drug pricing Issues related to the US manufacturing of pharmaceuticals Issues related to importation of drugs Issues related to direct-to-consumer drug delivery policy options Policies related to international reference pricing for pharmaceuticals Issues related to environmental sustainability Company sustainability policy issues FDA modernization policy issues Issues related to FDA Orange Book patent listings Pediatric rare disease priority review voucher Reauthorization of the pediatric priority review voucher program General issues related to health equity in rare disease and clinical trials General issues related to vaccine safety, efficacy, and access General issues related to rare disease and orphan drugs General issues related to ACIP recommendations Tariffs/trade policies related to tariffs on pharmaceuticals Most favored nation policies related to pharmaceuticals Issues related to a Most Favored Nations policy in Medicare and Medicaid Issues related to the Medicare title in the One Big Beautiful Bill Act

Centers for Medicare and Medicaid Innovation (CMMI) policy issues Value-based payment arrangements Medicare drug price negotiation Policies related to the use of international reference pricing in Medicare/Medicaid Most Favored Nation drug pricing proposals Issues related to e-labeling and allowing FDA to finalize a rule to allow digital versions of prescriptions Medicare patient access to rare disease therapies Part B and Part D drugs Medicare Part D reform and inflation penalties Medicare patient access to cancer screening Medicaid Drug Rebate Program proposed rule Definition of Qualified Single Source Drug (QSSD) for purposes of Medicare drug price negotiation E-labeling - allowing FDA to finalize a rule to allow digital versions of prescriptions Issues related to the digital communication of prescribing information for drugs Efforts to improve coding, coverage, and access for rare disease therapies General issues related to diagnostic reimbursement

E-labeling (allowing health care providers to receive prescribing information for drugs electronically rather than in paper form from manufacturers) Issues related to increasing production of US manufacturing

HR 591 - Defending American Jobs and Investment Act HR 1414 - Camerons Law, to restore orphan drug research tax credit HR 1990 - American Innovation and R&D Competitiveness Act of 2025 HR 2423 - Unfair Tax Prevention Act S 1605 - International Competition for American Jobs Act Expiring provisions of the Tax Cut and Jobs Act law - deduction of research and development expenditures Tax reform in budget reconciliation and Byrd rules Issues related to proposed Sec. 899 Issues related to international tax rules (GILTI/FDII/BEAT) Tariffs (general education, country-specific tariffs, sector-specific tariffs) Issues related to the renewable energy tax credits and other energy credits included in the Inflation Reduction Act Education on tax in preparation for 2025 tax legislation

Issues related to patents and intellectual property Issues related to FDA Orange Book patent listings

S.998 - Medical Supply Chain Resiliency Act Trade and tariffs (general education, country-specific tariffs, sector-specific tariffs) Pharmaceutical manufacturing (general education)

 Bills named in this filing 9
  • H.R. 1
    One Big Beautiful Bill Act
  • H.R. 946
    ORPHAN Cures Act
  • H.R. 1262
    Mikaela Naylon Give Kids a Chance Act
  • H.R. 1503
    Prescription Information Modernization Act of 2023
  • H.R. 591
    Defending American Jobs and Investment Act
  • H.R. 1414
    Cameron’s Law
  • H.R. 1990
    American Innovation and R&D Competitiveness Act of 2025
  • H.R. 2423
    Unfair Tax Prevention Act
  • S. 998
    Medical Supply Chain Resiliency Act

Source: federal Lobbying Disclosure Act filing, reproduced as filed. Bills are parsed from the activity descriptions.

Report a problem