Register entry

Vantage Specialty Ingredients, Inc.

Data as of · How to read this entry

Registered sites
1
Active NDC listings
5
Live patents
0
Countries
1
Base
United States
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Vantage Specialty Ingredients, Inc.707 Harco Dr, Englewood, Ohio (OH) 45315, United States (USA)Active ingredient (API) manufacture0001522195117509092
Catalogue

Drug listings by form and route

5

5 active NDC listings: 3 drug for further processing, 2 bulk ingredient. By marketing category: DRUG FOR FURTHER PROCESSING 3, BULK INGREDIENT 2.

Dosage formNDCs
gel4
liquid1
RouteNDCs
Labeller name on the listingNDCs
vantage specialty ingredients, inc.5
Catalogue

Marketed products

5
BrandGeneric nameForm / routeNDC
-BENZOYL PEROXIDEgel47643-001DRUG FOR FURTHER PROCESSING
-BENZOYL PEROXIDEgel47643-002DRUG FOR FURTHER PROCESSING
-BENZOYL PEROXIDEgel47643-003DRUG FOR FURTHER PROCESSING
-GLYCERINliquid47643-007BULK INGREDIENT
-SALICYLIC ACIDgel47643-004BULK INGREDIENT
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Comparable companies in United States

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Common questions

Is Vantage Specialty Ingredients, Inc. FDA approved?
Vantage Specialty Ingredients, 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 Vantage Specialty Ingredients, Inc.'s drugs manufactured?
The FDA register lists Englewood, OH. Registered operations: active ingredient (API) manufacture.
What drugs does Vantage Specialty Ingredients, Inc. make?
5 products are listed under Vantage Specialty Ingredients, Inc. in the openFDA NDC Directory, most often as gel; liquid. 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.