Register entry

Rapha Pharmaceuticals, Inc.

Data as of · How to read this entry

Registered sites
0
Active NDC listings
6
Live patents
0
Countries
0
Catalogue

Drug listings by form and route

6

6 active NDC listings: 6 human otc drug. By marketing category: ANDA 6.

Dosage formNDCs
tablet6
RouteNDCs
oral6
Labeller name on the listingNDCs
rapha pharmaceuticals, inc.6
Catalogue

Marketed products

6
BrandGeneric nameForm / routeNDC
Morning AfterLevonorgestreltablet, oral69953-515ANDA
Morning AfterLevonorgestreltablet, oral69953-516ANDA
Morning AfterLevonorgestreltablet, oral69953-517ANDA
PostDay One-StepLevonorgestreltablet, oral69953-617ANDA
PostDay One-StepLevonorgestreltablet, oral69953-618ANDA
PostDay One-StepLevonorgestreltablet, oral69953-628ANDA
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Other companies listing levonorgestrel

Enquiry

Common questions

Is Rapha Pharmaceuticals, Inc. FDA approved?
Rapha Pharmaceuticals, Inc. holds no registered establishment of its own; 6 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does Rapha Pharmaceuticals, Inc. make?
6 products are listed under Rapha Pharmaceuticals, Inc. 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.