Register entry

Analog Pharma

Data as of · How to read this entry

Registered sites
0
Active NDC listings
5
Live patents
0
Countries
0
Catalogue

Drug listings by form and route

5

5 active NDC listings: 5 human prescription drug. By marketing category: ANDA 4, NDA AUTHORIZED GENERIC 1.

Dosage formNDCs
capsule4
tablet, delayed release1
RouteNDCs
oral5
Labeller name on the listingNDCs
analog pharma5
Catalogue

Marketed products

5
BrandGeneric nameForm / routeNDC
Doxylamine succinate and pyridoxine hydrochlorideDoxylamine succinate and pyridoxine hydrochloridetablet, delayed release, oral70505-100NDA AUTHORIZED GENERIC
NitisinoneNitisinonecapsule, oral70505-202ANDA
NitisinoneNitisinonecapsule, oral70505-205ANDA
NitisinoneNitisinonecapsule, oral70505-210ANDA
NitisinoneNitisinonecapsule, oral70505-220ANDA
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Other companies listing nitisinone

Enquiry

Common questions

Is Analog Pharma FDA approved?
Analog Pharma holds no registered establishment of its own; 5 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does Analog Pharma make?
5 products are listed under Analog Pharma in the openFDA NDC Directory, most often as capsule; tablet, delayed release. 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.