Register entry

Umasuto, LLC

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Registered sites
0
Active NDC listings
7
Live patents
0
Countries
0
Catalogue

Drug listings by form and route

7

7 active NDC listings: 6 human prescription drug, 1 human otc drug. By marketing category: ANDA 7.

Dosage formNDCs
tablet7
RouteNDCs
oral7
Labeller name on the listingNDCs
umasuto, llc7
Catalogue

Marketed products

7
BrandGeneric nameForm / routeNDC
Cetirizine HydrochlorideCetirizine Hydrochloridetablet, oral85293-001ANDA
Midodrine HydrochlorideMidodrine Hydrochloridetablet, oral85293-005ANDA
Midodrine HydrochlorideMidodrine Hydrochloridetablet, oral85293-006ANDA
Midodrine HydrochlorideMidodrine Hydrochloridetablet, oral85293-007ANDA
ciprofloxacinciprofloxacintablet, oral85293-002ANDA
ciprofloxacinciprofloxacintablet, oral85293-003ANDA
ciprofloxacinciprofloxacintablet, oral85293-004ANDA
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Other companies listing midodrine hydrochloride

Enquiry

Common questions

Is Umasuto, LLC FDA approved?
Umasuto, LLC holds no registered establishment of its own; 7 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does Umasuto, LLC make?
7 products are listed under Umasuto, LLC in the openFDA NDC Directory, most often as tablet. 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.