Register entryRepackager / relabeller

PharmPak, Inc.

Data as of · How to read this entry

Registered sites
1
Active NDC listings
23
Labeller names
2
Live patents
0
Countries
1
Base
United States
Authorisation

Registered operations

Relabelling1Repackaging1
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
PharmPak, Inc.1221 Andersen Drive Suite B, San Rafael, California (CA) 94901, United States (USA)Relabelling, Repackaging2938360175493840
Catalogue

Drug listings by form and route

23

23 active NDC listings: 23 human prescription drug. By marketing category: ANDA 22, NDA 1.

Dosage formNDCs
tablet14
tablet, film coated8
capsule1
RouteNDCs
oral23
Labeller name on the listingNDCs
pharmpak, inc.22
pharmpak, inc.1
Catalogue

Marketed products

23
BrandGeneric nameForm / routeNDC
AcyclovirACYCLOVIRtablet, oral54348-624ANDA
AcyclovirAcyclovirtablet, oral54348-627ANDA
AzithromycinAZITHROMYCIN MONOHYDRATEtablet, film coated, oral54348-857ANDA
EstradiolESTRADIOLtablet, oral54348-701ANDA
EstradiolESTRADIOLtablet, oral54348-702ANDA
IbuprofenIBUPROFENtablet, film coated, oral54348-825ANDA
IbuprofenIBUPROFENtablet, film coated, oral54348-830ANDA
IbuprofenIBUPROFENtablet, film coated, oral54348-835ANDA
LorazepamLORAZEPAMtablet, oral54348-049ANDA
MedroxyprogesteroneMEDROXYPROGESTERONEtablet, oral54348-805ANDA
MetronidazoleMETRONIDAZOLEtablet, film coated, oral54348-740ANDA
MetronidazoleMETRONIDAZOLEtablet, film coated, oral54348-745ANDA
MisoprostolMISOPROSTOLtablet, oral54348-148ANDA
Nitrofurantoin MonoNITROFURANTOIN MONOHYDRATEcapsule, oral54348-849NDA
OndansetronONDANSETRONtablet, film coated, oral54348-819ANDA
Ondansetron HydrochlorideOndansetron Hydrochloridetablet, film coated, oral54348-821ANDA
PrednisonePREDNISONEtablet, oral54348-506ANDA
ProchlorperazinePROCHLORPERAZINEtablet, oral54348-989ANDA
PromethazinePROMETHAZINEtablet, oral54348-117ANDA
SpironolactoneSPIRONOLACTONEtablet, oral54348-340ANDA
Sulfamethox-TMP DSSULFAMETHOXAZOLE, TRIMETHOPRIMtablet, oral54348-625ANDA
ciprofloxacinCIPROFLOXACINtablet, oral54348-662ANDA
ciprofloxacinCIPROFLOXACINtablet, oral54348-663ANDA
Neighbours

Registered in the same town

2
Compare

Comparable companies in United States

Enquiry

Common questions

Is PharmPak, Inc. FDA approved?
PharmPak, 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 PharmPak, Inc.'s registered sites?
The FDA register lists San Rafael, CA. Registered operations: relabelling, repackaging.
What drugs does PharmPak, Inc. make?
23 products are listed under PharmPak, Inc. in the openFDA NDC Directory, most often as tablet; tablet, film coated; capsule. 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.