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Foreign-Trade Zone (FTZ) 7-Mayaguez, Puerto Rico, Notification of Proposed Production Activity, AbbVie Ltd., (Pharmaceutical Products), Barceloneta, Puerto Rico

---
identifier: "/us/fr/2022-10746"
source: "fr"
legal_status: "authoritative_unofficial"
title: "Foreign-Trade Zone (FTZ) 7-Mayaguez, Puerto Rico, Notification of Proposed Production Activity, AbbVie Ltd., (Pharmaceutical Products), Barceloneta, Puerto Rico"
title_number: 0
title_name: "Federal Register"
section_number: "2022-10746"
section_name: "Foreign-Trade Zone (FTZ) 7-Mayaguez, Puerto Rico, Notification of Proposed Production Activity, AbbVie Ltd., (Pharmaceutical Products), Barceloneta, Puerto Rico"
positive_law: false
currency: "2022-05-19"
last_updated: "2022-05-19"
format_version: "1.1.0"
generator: "[email protected]"
agency: "Commerce Department"
document_number: "2022-10746"
document_type: "notice"
publication_date: "2022-05-19"
agencies:
  - "Commerce Department"
  - "Foreign-Trade Zones Board"
fr_citation: "87 FR 30448"
fr_volume: 87
docket_ids:
  - "B-19-2022"
---

#  Foreign-Trade Zone (FTZ) 7—Mayaguez, Puerto Rico, Notification of Proposed Production Activity, AbbVie Ltd., (Pharmaceutical Products), Barceloneta, Puerto Rico

AbbVie Ltd., submitted a notification of proposed production activity to the FTZ Board (the Board) for its facility in Barceloneta, Puerto Rico within Subzone 7I. The notification conforming to the requirements of the Board's regulations (15 CFR 400.22) was received on May 13, 2022.

Pursuant to 15 CFR 400.14(b), FTZ production activity would be limited to the specific foreign-status material and specific finished product described in the submitted notification (summarized below) and subsequently authorized by the Board. The benefits that may stem from conducting production activity under FTZ procedures are explained in the background section of the Board's website—accessible via *www.trade.gov/ftz.* The proposed finished product and material would be added to the production authority that the Board previously approved for the operation, as reflected on the Board's website.

The proposed finished product is venetoclax film coated tablets (duty-free).

The proposed foreign-status material is venetoclax active pharmaceutical ingredient (duty rate 6.5%).

Public comment is invited from interested parties. Submissions shall be addressed to the Board's Executive Secretary and sent to: *[email protected].* The closing period for their receipt is June 28, 2022.

A copy of the notification will be available for public inspection in the “Online FTZ Information System” section of the Board's website.

For further information, contact Christopher Wedderburn at *[email protected].*

Dated: May 13, 2022.

Elizabeth Whiteman,

Acting Executive Secretary.