Register entryRepackager / relabeller

Cranbury Pharmaceuticals Inc

Data as of · How to read this entry

Registered sites
1
Active NDC listings
44
Live patents
0
Countries
1
Base
United States
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Cranbury Pharmaceuticals, Inc.Registrant: Cranbury Pharmaceuticals Inc2031 Route 130, MONMOUTH JUNCTION, New Jersey (NJ) 08852, United States (USA)Relabelling3010241920078889499
Catalogue

Drug listings by form and route

44

44 active NDC listings: 44 human prescription drug. By marketing category: ANDA 44.

Dosage formNDCs
tablet18
solution10
tablet, film coated5
capsule4
tablet, extended release4
suspension1
suspension, extended release1
syrup1
RouteNDCs
oral44
Labeller name on the listingNDCs
cranbury pharmaceuticals, llc44
Catalogue

Marketed products

44
BrandGeneric nameForm / routeNDC
CABERGOLINECABERGOLINEtablet, oral27808-315ANDA
CelecoxibCelecoxibcapsule, oral27808-295ANDA
CelecoxibCelecoxibcapsule, oral27808-296ANDA
CelecoxibCelecoxibcapsule, oral27808-297ANDA
Colesevelam hydrochlorideColesevelam hydrochloridetablet, oral27808-190ANDA
DOXYCYCLINE HYCLATEDOXYCYCLINE HYCLATEtablet, oral27808-234ANDA
Deflazacort Oral SuspensionDeflazacort Oralsuspension, oral27808-249ANDA
Dexmethylphenidate Hydrochloridedexmethylphenidate hydrochloridetablet, oral27808-091ANDA
Dexmethylphenidate Hydrochloridedexmethylphenidate hydrochloridetablet, oral27808-092ANDA
Dexmethylphenidate Hydrochloridedexmethylphenidate hydrochloridetablet, oral27808-093ANDA
DextroamphetamineDextroamphetaminesolution, oral27808-085ANDA
Dextroamphetamine SulfateDextroamphetamine Sulfatetablet, oral27808-089ANDA
Dextroamphetamine SulfateDextroamphetamine Sulfatetablet, oral27808-090ANDA
Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophentablet, oral27808-035ANDA
Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophentablet, oral27808-036ANDA
Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophentablet, oral27808-037ANDA
Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophensolution, oral27808-049ANDA
Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophentablet, oral27808-114ANDA
Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophentablet, oral27808-115ANDA
Hydrocodone Bitartrate and AcetaminophenHydrocodone Bitartrate and Acetaminophentablet, oral27808-116ANDA
Hydrocodone Polistirex and Chlorpheniramine Polistirex extended-releaseHydrocodone Polistirex and Chlorpheniramine Polistirexsuspension, extended release, oral27808-086ANDA
LevetiracetamLevetiracetamtablet, oral27808-263ANDA
LevetiracetamLevetiracetamtablet, oral27808-264ANDA
LevetiracetamLevetiracetamtablet, oral27808-265ANDA
LevetiracetamLevetiracetamtablet, oral27808-266ANDA
Methylphenidate HydrochlorideMethylphenidate Hydrochloridesolution, oral27808-058ANDA
Methylphenidate HydrochlorideMethylphenidate Hydrochloridesolution, oral27808-059ANDA
Metoprolol SuccinateMetoprolol Succinatetablet, extended release, oral27808-302ANDA
Metoprolol SuccinateMetoprolol Succinatetablet, extended release, oral27808-303ANDA
Metoprolol SuccinateMetoprolol Succinatetablet, extended release, oral27808-304ANDA
Metoprolol SuccinateMetoprolol Succinatetablet, extended release, oral27808-305ANDA
Morphine SulfateMorphine Sulfatesolution, oral27808-082ANDA
Promethazine Hydrochloride and Codeine PhosphatePromethazine Hydrochloride and Codeine Phosphatesolution, oral27808-065ANDA
Promethazine Hydrochloride and Dextromethorphan HydrobromidePromethazine Hydrochloride and Dextromethorphan Hydrobromidesolution, oral27808-057ANDA
RisperidoneRisperidonesolution, oral27808-002ANDA
Rosuvastatin CalciumRosuvastatin Calciumtablet, film coated, oral27808-155ANDA
Rosuvastatin CalciumRosuvastatin Calciumtablet, film coated, oral27808-156ANDA
Rosuvastatin CalciumRosuvastatin Calciumtablet, film coated, oral27808-157ANDA
Rosuvastatin CalciumRosuvastatin Calciumtablet, film coated, oral27808-158ANDA
TRAMADOL HYDROCHLORIDETRAMADOL HYDROCHLORIDEtablet, film coated, oral27808-301ANDA
TheophyllineTheophyllinesolution, oral27808-033ANDA
doxycyclinedoxycyclinecapsule, oral27808-233ANDA
hydrocodone bitartrate and acetaminophenhydrocodone bitartrate and acetaminophensolution, oral27808-130ANDA
promethazine hydrochloridepromethazine hydrochloridesyrup, oral27808-051ANDA
Neighbours

Registered in the same town

2
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Comparable companies in United States

Enquiry

Common questions

Is Cranbury Pharmaceuticals Inc FDA approved?
Cranbury Pharmaceuticals 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 Cranbury Pharmaceuticals Inc's registered sites?
The FDA register lists MONMOUTH JUNCTION, NJ. Registered operations: relabelling.
What drugs does Cranbury Pharmaceuticals Inc make?
44 products are listed under Cranbury Pharmaceuticals Inc in the openFDA NDC Directory, most often as tablet; solution; tablet, film coated. 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.