Medical Products Laboratories, 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
- 9990 Global Road, Philadelphia, Pennsylvania (PA) 19115, United States (USA)
- Operations here
- analysislabelmanufacturepackrelabelrepack
- FDA identifiers
- FEI 2513595 · DUNS 002290302
FDA inspection history
Outcomes of closed FDA inspections at this site (drug and biologic program areas).
- VAIDrug Quality Assurance2023-07-13
- VAIDrug Quality Assurance2020-03-13
- VAIDrug Quality Assurance2017-10-12
- VAIDrug Quality Assurance2015-07-21
- VAIDrug Quality Assurance2014-02-24
- NAIDrug Quality Assurance2011-07-13
- VAIDrug Quality Assurance2011-04-27
- VAIDrug Quality Assurance2010-06-14
Drugs this plant is listed as making
5 distinct drugs across 10 products name this site in their FDA label.
- Aluminium Chloride HexahydrateMedical Products Laboratories, Inc.
- HydroquinoneDermavance Pharmaceuticals
- Sodium FluorideDmg America, Llc
- Sulfacetamide SodiumBioComp Pharma, Inc.
- Sulfacetamide Sodium, SulfurBioComp Pharma, Inc.
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.