Renaissance Lakewood LLC
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
- 1200 Paco Way, Lakewood, New Jersey (NJ) 08701, United States (USA)
- Operations here
- analysislabelmanufacturepack
- FDA identifiers
- FEI 2242829 · DUNS 077744035
FDA inspection history
Outcomes of closed FDA inspections at this site (drug and biologic program areas).
- VAIDrug Quality Assurance2023-06-06
- VAIDrug Quality Assurance2019-08-22
- VAIDrug Quality Assurance2018-03-15
- NAIDrug Quality Assurance2017-04-26
- NAIDrug Quality Assurance2016-06-01
- VAIDrug Quality Assurance2015-02-06
- NAIDrug Quality Assurance2014-11-04
- NAIDrug Quality Assurance2013-01-17
- OAIDrug Quality Assurance2012-03-07
- VAIDrug Quality Assurance2011-08-10
- NAIDrug Quality Assurance2010-06-15
- VAIDrug Quality Assurance2010-04-28
- NAIDrug Quality Assurance2009-11-03
Drugs this plant is listed as making
3 distinct drugs across 3 products name this site in their FDA label.
- Collagenase SantylSmith & Nephew, Inc
- Succinylcholine ChlorideNordic Pharma, Inc.
- sumatriptanUpsher-Smith Laboratories, LLC
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.