PureTek Corporation
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
- 1145 Arroyo Ave Unit D, San Fernando, California (CA) 91340, United States (USA)
- Operations here
- analysislabelmanufacturepackrelabelrepack
- FDA identifiers
- FEI 1000125324 · DUNS 785961046
FDA inspection history
Outcomes of closed FDA inspections at this site (drug and biologic program areas).
- VAIDrug Quality Assurance2025-03-07
- VAIDrug Quality Assurance2020-01-30
- VAIDrug Quality Assurance2017-12-15
- VAIDrug Quality Assurance2015-10-27
- VAIUnapproved and Misbranded Drugs2015-10-27
- VAIDrug Quality Assurance2015-03-18
- VAIDrug Quality Assurance2013-12-18
- VAIDrug Quality Assurance2012-12-04
- NAIDrug Quality Assurance2011-01-21
- VAIDrug Quality Assurance2010-07-16
Drugs this plant is listed as making
20 distinct drugs across 26 products name this site in their FDA label.
- DimethiconePureTek Corporation
- Ferrous Fumarate, Folic AcidPureTek Corporation
- Ferrous Fumarate, Polysaccharide Iron ComplexPureTek Corporation
- fluocinonide, dimethiconePureTek Corporation
- Folic AcidPureTek Corporation
- Folic Acid, Vitamin D3PureTek Corporation
- GabapentinPureTek Corporation
- HydroquinoneObagi Cosmeceuticals LLC
- HYDROQUINONE, HOMOSALATE, OCTISALATE, and ZINC OXIDEObagi Cosmeceutical Llc
- Hydroquinone, Octisalate and Zinc OxideObagi Cosmeceutical Llc
- Hydroquinone, Titanium Dioxide, and Zinc OxideObagi Cosmeceuticals LLC
- IbuprofenPureTek Corporation
- Lidocaine Hcl - Hydrocortisone AcetatePureTek Corporation
- Lidocaine HCl and Hydrocortisone AcetatePureTek Corporation
- Lidocaine Hydrochloridein shortagePureTek Corporation
- lidocaine, dimethiconePureTek Corporation
- MethocarbamolPureTek Corporation
- Phenazopyridine HydrochlorideWinder Laboratories, LLC
- Triamcinolone AcetonidePureTek Corporation
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.