Register entryRepackager / relabeller
- Registered sites
- 1
- Active NDC listings
- 1
- Live patents
- 0
- Countries
- 1
- Base
- United States
Authorisation
Registered operations
Labelling1Packaging1
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| PEDIFIX, INC. | 301 Fields Ln, Brewster, New York (NY) 10509, United States (USA) | Labelling, Packaging | 3009710062122271935 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| PediFix Lidocaine Pain-Relief Patches | Lidocaine Pain-Relief Patches | patch, topical | 68927-3700OTC MONOGRAPH DRUG |
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Enquiry
Common questions
- Is PEDIFIX, INC. FDA approved?
- PEDIFIX, INC. holds 1 FDA-registered establishment in the United States. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
- Where are PEDIFIX, INC.'s registered sites?
- The FDA register lists Brewster, NY. Registered operations: labelling, packaging.
- What drugs does PEDIFIX, INC. make?
- 1 product is listed under PEDIFIX, INC. in the openFDA NDC Directory, most often as patch. The full breakdown by dosage form and route is above. A listing count is not a sales figure.
Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.