Register 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| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Carlsbad Technology, Inc. | 5922 FARNSWORTH CT, Carlsbad, California (CA) 92008, United States (USA) | Analytical testing, Labelling, Finished drug manufacture, Packaging | 1000135190781047246 |
Catalogue
Drug listings by form and route
2929 active NDC listings: 29 human prescription drug. By marketing category: ANDA 29.
| Dosage form | NDCs |
|---|---|
| tablet | 13 |
| tablet, film coated | 8 |
| tablet, delayed release | 5 |
| capsule | 3 |
| Route | NDCs |
|---|---|
| oral | 29 |
| Labeller name on the listing | NDCs |
|---|---|
| carlsbad technology, inc. | 27 |
| carlsbad technology, inc | 2 |
Catalogue
Marketed products
29| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Acyclovir | Acyclovir | tablet, oral | 61442-112ANDA |
| Acyclovir | Acyclovir | tablet, oral | 61442-113ANDA |
| Acyclovir | Acyclovir | capsule, oral | 61442-114ANDA |
| Cefaclor | Cefaclor | capsule, oral | 61442-171ANDA |
| Cefaclor | Cefaclor | capsule, oral | 61442-172ANDA |
| Ciprofloxacin | Ciprofloxacin Hydrochloride | tablet, film coated, oral | 61442-222ANDA |
| Ciprofloxacin | Ciprofloxacin Hydrochloride | tablet, film coated, oral | 61442-223ANDA |
| Ciprofloxacin | Ciprofloxacin Hydrochloride | tablet, film coated, oral | 61442-224ANDA |
| Diclofenac Sodium Delayed Release | Diclofenac Sodium | tablet, delayed release, oral | 61442-101ANDA |
| Diclofenac Sodium Delayed Release | Diclofenac Sodium | tablet, delayed release, oral | 61442-102ANDA |
| Diclofenac Sodium Delayed Release | Diclofenac Sodium | tablet, delayed release, oral | 61442-103ANDA |
| Diclofenac Sodium Delayed Release | Diclofenac Sodium | tablet, delayed release, oral | 61442-226ANDA |
| Diclofenac Sodium Delayed Release | Diclofenac Sodium | tablet, delayed release, oral | 61442-227ANDA |
| Entecavir | Entecavir | tablet, oral | 61442-311ANDA |
| Famotidine | Famotidine | tablet, oral | 61442-121ANDA |
| Famotidine | Famotidine | tablet, oral | 61442-122ANDA |
| Felodipine | Felodipine | tablet, film coated, oral | 61442-431ANDA |
| Felodipine | Felodipine | tablet, film coated, oral | 61442-432ANDA |
| Felodipine | Felodipine | tablet, film coated, oral | 61442-433ANDA |
| Glimepiride | Glimepiride | tablet, oral | 61442-115ANDA |
| Glimepiride | Glimepiride | tablet, oral | 61442-116ANDA |
| Glimepiride | Glimepiride | tablet, oral | 61442-117ANDA |
| Lovastatin | Lovastatin | tablet, oral | 61442-141ANDA |
| Lovastatin | Lovastatin | tablet, oral | 61442-142ANDA |
| Lovastatin | Lovastatin | tablet, oral | 61442-143ANDA |
| Meloxicam | Meloxicam | tablet, oral | 61442-126ANDA |
| Meloxicam | Meloxicam | tablet, oral | 61442-127ANDA |
| Memantine Hydrochloride | Memantine Hydrochloride | tablet, film coated, oral | 61442-192ANDA |
| Memantine Hydrochloride | Memantine Hydrochloride | tablet, film coated, oral | 61442-193ANDA |
Neighbours
Registered in the same town
3- Sigma-Aldrich CorporationCarlsbad, CA · 2 sites
- Novartis Pharmaceuticals CorporationCarlsbad, CA
- Ionis Pharmaceuticals Inc.Carlsbad, CA
Compare
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- HF Acquisition Co LLC1 site · 363 NDC
- ANI Pharmaceuticals, Inc.1 site · 299 NDC
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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.