Register entry
- Registered sites
- 1
- Active NDC listings
- 1
- Live patents
- 0
- Countries
- 1
- Base
- Brazil
Authorisation
Registered operations
Analytical testing1Active ingredient (API) manufacture1Labelling1
Sites
Registered establishments
1| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Anidro Do Brasil Extracoes SA | Rua Pilocarpina 1000, Parnaiba, Piaui 64216-815, Brazil (BRA) | Analytical testing, Active ingredient (API) manufacture, Labelling | 3002807563901780295 |
Catalogue
Marketed products
1| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| - | Pilocarpine HCl | powder | 58574-001BULK INGREDIENT |
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Enquiry
Common questions
- Is Anidro Do Brasil Extracoes SA FDA approved?
- Anidro Do Brasil Extracoes SA holds 1 FDA-registered establishment in Brazil. 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 Anidro Do Brasil Extracoes SA's drugs manufactured?
- The FDA register lists Parnaiba. Registered operations: analytical testing, active ingredient (API) manufacture, labelling.
- What drugs does Anidro Do Brasil Extracoes SA make?
- 1 product is listed under Anidro Do Brasil Extracoes SA in the openFDA NDC Directory, most often as powder. 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.