Register entry
Avista Pharma Solutions, Inc. dba Cambrex
Data as of · How to read this entry
- Registered sites
- 3
- Active NDC listings
- 0
- Live patents
- 0
- Countries
- 1
- Base
- United States
Authorisation
Registered operations
Analytical testing3Active ingredient (API) manufacture1Finished drug manufacture2
Sites
Registered establishments
3| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Avista Pharma Solutions, Inc. dba Cambrex | 104 Gold St, Agawam, Massachusetts (MA) 01001-3807, United States (USA) | Analytical testing | 1220785079509111 |
| Avista Pharma Solutions, Inc. dba Cambrex | 3501 Tricenter Blvd Ste C, Durham, North Carolina (NC) 27713-1868, United States (USA) | Analytical testing, Finished drug manufacture | 3011795391108353231 |
| Avista Pharma Solutions, Inc. dba Cambrex | 2620 Trade Centre Ave., Longmont, Colorado (CO) 80503-7551, United States (USA) | Analytical testing, Active ingredient (API) manufacture, Finished drug manufacture | 3012316957144616641 |
Neighbours
Registered in the same town
12- Almac Clinical Services, LLCDurham, NC · 3 sites
- Merck & Co., Inc.Durham, NC · 2 sites
- KBI Biopharma, Inc.Durham, NC · 2 sites
- PETNET Solutions, Inc.DURHAM, NC
- Novo Nordisk Inc.Durham, NC
- Eli Lilly and CompanyDurham, NC
- AGC Biologics, Inc.Longmont, CO
- Encube Ethicals LimitedDurham, NC
- Oxford Biomedica (UK) LimitedDurham, NC
- United Therapeutics CorporationDurham, NC
- Aurolife Pharma LLCDurham, NC
- BioAgilytix Labs, LLCDurham, NC
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Enquiry
Common questions
- Is Avista Pharma Solutions, Inc. dba Cambrex FDA approved?
- Avista Pharma Solutions, Inc. dba Cambrex holds 3 FDA-registered establishments 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 Avista Pharma Solutions, Inc. dba Cambrex's drugs manufactured?
- The FDA register lists Agawam, MA; Durham, NC; Longmont, CO. Registered operations: analytical testing, active ingredient (API) manufacture, finished drug manufacture.
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.