Register entry

Carlsbad Technology, Inc.

Data as of · How to read this entry

Registered sites
1
Active NDC listings
29
Labeller names
2
Live patents
0
Countries
1
Base
United States
Authorisation

Registered operations

Analytical testing1Labelling1Finished drug manufacture1Packaging1
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Carlsbad Technology, Inc.5922 FARNSWORTH CT, Carlsbad, California (CA) 92008, United States (USA)Analytical testing, Labelling, Finished drug manufacture, Packaging1000135190781047246
Catalogue

Drug listings by form and route

29

29 active NDC listings: 29 human prescription drug. By marketing category: ANDA 29.

Dosage formNDCs
tablet13
tablet, film coated8
tablet, delayed release5
capsule3
RouteNDCs
oral29
Labeller name on the listingNDCs
carlsbad technology, inc.27
carlsbad technology, inc2
Catalogue

Marketed products

29
BrandGeneric nameForm / routeNDC
AcyclovirAcyclovirtablet, oral61442-112ANDA
AcyclovirAcyclovirtablet, oral61442-113ANDA
AcyclovirAcyclovircapsule, oral61442-114ANDA
CefaclorCefaclorcapsule, oral61442-171ANDA
CefaclorCefaclorcapsule, oral61442-172ANDA
CiprofloxacinCiprofloxacin Hydrochloridetablet, film coated, oral61442-222ANDA
CiprofloxacinCiprofloxacin Hydrochloridetablet, film coated, oral61442-223ANDA
CiprofloxacinCiprofloxacin Hydrochloridetablet, film coated, oral61442-224ANDA
Diclofenac Sodium Delayed ReleaseDiclofenac Sodiumtablet, delayed release, oral61442-101ANDA
Diclofenac Sodium Delayed ReleaseDiclofenac Sodiumtablet, delayed release, oral61442-102ANDA
Diclofenac Sodium Delayed ReleaseDiclofenac Sodiumtablet, delayed release, oral61442-103ANDA
Diclofenac Sodium Delayed ReleaseDiclofenac Sodiumtablet, delayed release, oral61442-226ANDA
Diclofenac Sodium Delayed ReleaseDiclofenac Sodiumtablet, delayed release, oral61442-227ANDA
EntecavirEntecavirtablet, oral61442-311ANDA
FamotidineFamotidinetablet, oral61442-121ANDA
FamotidineFamotidinetablet, oral61442-122ANDA
FelodipineFelodipinetablet, film coated, oral61442-431ANDA
FelodipineFelodipinetablet, film coated, oral61442-432ANDA
FelodipineFelodipinetablet, film coated, oral61442-433ANDA
GlimepirideGlimepiridetablet, oral61442-115ANDA
GlimepirideGlimepiridetablet, oral61442-116ANDA
GlimepirideGlimepiridetablet, oral61442-117ANDA
LovastatinLovastatintablet, oral61442-141ANDA
LovastatinLovastatintablet, oral61442-142ANDA
LovastatinLovastatintablet, oral61442-143ANDA
MeloxicamMeloxicamtablet, oral61442-126ANDA
MeloxicamMeloxicamtablet, oral61442-127ANDA
Memantine HydrochlorideMemantine Hydrochloridetablet, film coated, oral61442-192ANDA
Memantine HydrochlorideMemantine Hydrochloridetablet, film coated, oral61442-193ANDA
Neighbours

Registered in the same town

3
Compare

Comparable companies in United States

Enquiry

Common questions

Is Carlsbad Technology, Inc. FDA approved?
Carlsbad Technology, 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 Carlsbad Technology, Inc.'s drugs manufactured?
The FDA register lists Carlsbad, CA. Registered operations: analytical testing, labelling, finished drug manufacture, packaging.
What drugs does Carlsbad Technology, Inc. make?
29 products are listed under Carlsbad Technology, Inc. in the openFDA NDC Directory, most often as tablet; tablet, film coated; tablet, delayed release. 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.