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PA HB 2749: An Act amending the act of April 14, 1972 (P.L.233, No.64), known as The Controlled Substance, Drug, Device and Cosmetic Act, further providing for drug overdose medication.

Detected August 26, 2026 · in Pharmaceutical Manufacturing (FDA/DEA)

PA HB 2749 proposes amendments to the Controlled Substance, Drug, Device and Cosmetic Act regarding drug overdose medication, but the excerpt is empty, so specific changes are unknown.

Aforeworn detected this change in the Pharmaceutical Manufacturing (FDA/DEA) space on August 26, 2026 and published this briefing so affected operators are forewarned rather than caught off guard. It is rated Low urgency. Pharmaceutical manufacturers, including branded, generic, API, and compounding outsourcing facilities operating in Pennsylvania. should confirm how it applies to their specific situation before acting. There is a time constraint attached: Not specified; bill is in early legislative stage.. Acting after that point can mean penalties, a lapsed licence, or lost eligibility — exactly the kind of surprise Aforeworn exists to prevent. Aforeworn monitors Pharmaceutical Manufacturing (FDA/DEA) continuously and turns every detected change into a plain-English briefing like this one, so you always know first. Forewarned is forearmed.

What changed

The bill would amend the Controlled Substance, Drug, Device and Cosmetic Act to address drug overdose medication, but the specific provisions are not yet available.

Who it affects

Pharmaceutical manufacturers, including branded, generic, API, and compounding outsourcing facilities operating in Pennsylvania.

What you must do

Monitor the bill's progress and review the full text when available to assess potential impacts on manufacturing and distribution practices.

Deadline

Not specified; bill is in early legislative stage.

Source: https://www.palegis.us/legislation/bills

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