Actavis Laboratories FL, Inc.
A single plant registered with the FDA to make drugs for the US market. Below is where it is and the drugs whose FDA labels list this site as performing a manufacturing step — so if this plant has a problem, these are the products that could be affected.
- Country
- United States
- Registered address
- 4955 Orange Drive, Davie, Florida (FL) 33314, United States (USA)
- Operations here
- analysismanufacturepack
- FDA identifiers
- FEI 3003194604 · DUNS 020778751
FDA inspection history
Outcomes of closed FDA inspections at this site (drug and biologic program areas).
- VAIDrug Quality Assurance2025-11-18
- VAIDrug Quality Assurance2021-05-25
- OAIDrug Quality Assurance2020-01-17
- OAIDrug Quality Assurance2018-07-19
- VAIDrug Quality Assurance2017-11-28
- VAIDrug Quality Assurance2016-01-15
- VAIDrug Quality Assurance2013-12-20
- VAIDrug Quality Assurance2011-04-25
- VAIDrug Quality Assurance2009-09-04
Drugs this plant is listed as making
1 distinct drugs across 2 products name this site in their FDA label.
- Diclofenac Sodium and MisoprostolBluePoint Laboratories
Sources:the establishment's name, address, and country from FDA's Drug Establishments Current Registration Site (DECRS); the drug-to-facility links from DailyMed SPL drug labels, matched by the facility's DUNS number; inspection outcomes from the FDA Data Dashboard, matched by FEI; shortage status from FDA's drug shortage database. More on how this is built. Educational only.