Register entry

Modavar Pharmaceuticals LLC

Data as of · How to read this entry

Registered sites
1
Active NDC listings
59
Live patents
0
Countries
1
Base
United States
Authorisation

Registered operations

Analytical testing1Labelling1Finished drug manufacture1Packaging1
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Modavar PharmaceuticalsRegistrant: Modavar Pharmaceuticals LLC4600 Wedgewood Blvd Ste, Frederick, Maryland (MD) 21703, United States (USA)Analytical testing, Labelling, Finished drug manufacture, Packaging3014525970960937030
Catalogue

Drug listings by form and route

59

59 active NDC listings: 59 human prescription drug. By marketing category: ANDA 59.

Dosage formNDCs
tablet22
capsule15
tablet, film coated10
tablet, coated9
tablet, film coated, extended release3
RouteNDCs
oral59
Labeller name on the listingNDCs
modavar pharmaceuticals llc59
Catalogue

Marketed products

59
BrandGeneric nameForm / routeNDC
AcyclovirAcyclovirtablet, oral72241-026ANDA
AcyclovirAcyclovirtablet, oral72241-027ANDA
AcyclovirAcyclovircapsule, oral72241-028ANDA
Bupropion HydrochlorideBupropion Hydrochloridetablet, film coated, oral72241-020ANDA
Bupropion HydrochlorideBupropion Hydrochloridetablet, film coated, oral72241-021ANDA
CelecoxibCelecoxibcapsule, oral72241-022ANDA
CelecoxibCelecoxibcapsule, oral72241-023ANDA
CelecoxibCelecoxibcapsule, oral72241-024ANDA
CelecoxibCelecoxibcapsule, oral72241-025ANDA
ErythromycinErythromycintablet, film coated, oral72241-036ANDA
ErythromycinErythromycintablet, film coated, oral72241-037ANDA
FluoxetineFluoxetinecapsule, oral72241-007ANDA
FluoxetineFluoxetinecapsule, oral72241-008ANDA
FluoxetineFluoxetinecapsule, oral72241-009ANDA
Folic AcidFolic Acidtablet, oral72241-050ANDA
GlyburideGlyburidetablet, oral72241-038ANDA
GlyburideGlyburidetablet, oral72241-039ANDA
GlyburideGlyburidetablet, oral72241-040ANDA
HYDRALAZINE HYDROCHLORIDEhydralazine hydrochloridetablet, oral72241-004ANDA
HYDRALAZINE HYDROCHLORIDEhydralazine hydrochloridetablet, oral72241-005ANDA
HYDRALAZINE HYDROCHLORIDEhydralazine hydrochloridetablet, oral72241-006ANDA
NateglinideNateglinidetablet, coated, oral72241-002ANDA
NateglinideNateglinidetablet, coated, oral72241-003ANDA
NebivololNebivololtablet, oral72241-032ANDA
NebivololNebivololtablet, oral72241-033ANDA
NebivololNebivololtablet, oral72241-034ANDA
NebivololNebivololtablet, oral72241-035ANDA
OFLOXACINOFLOXACINtablet, film coated, oral72241-072ANDA
OFLOXACINOFLOXACINtablet, film coated, oral72241-073ANDA
OFLOXACINOFLOXACINtablet, film coated, oral72241-074ANDA
OlanzapineOlanzapinetablet, oral72241-051ANDA
OlanzapineOlanzapinetablet, oral72241-052ANDA
OlanzapineOlanzapinetablet, oral72241-053ANDA
OlanzapineOlanzapinetablet, oral72241-054ANDA
OlanzapineOlanzapinetablet, oral72241-055ANDA
OlanzapineOlanzapinetablet, oral72241-056ANDA
Olmesartan MedoxomilOlmesartan Medoxomiltablet, coated, oral72241-078ANDA
Olmesartan MedoxomilOlmesartan Medoxomiltablet, coated, oral72241-079ANDA
Olmesartan MedoxomilOlmesartan Medoxomiltablet, coated, oral72241-080ANDA
ParoxetineParoxetinetablet, film coated, extended release, oral72241-029ANDA
ParoxetineParoxetinetablet, film coated, extended release, oral72241-030ANDA
ParoxetineParoxetinetablet, film coated, extended release, oral72241-031ANDA
Raloxifene hydrochlorideRaloxifene hydrochloridetablet, coated, oral72241-010ANDA
Rivastigmine TartrateRivastigmine Tartratecapsule, oral72241-011ANDA
Rivastigmine TartrateRivastigmine Tartratecapsule, oral72241-012ANDA
Rivastigmine TartrateRivastigmine Tartratecapsule, oral72241-013ANDA
Rivastigmine TartrateRivastigmine Tartratecapsule, oral72241-014ANDA
SildenafilSildenafiltablet, film coated, oral72241-069ANDA
SildenafilSildenafiltablet, film coated, oral72241-070ANDA
SildenafilSildenafiltablet, film coated, oral72241-071ANDA
TelmisartanTelmisartantablet, oral72241-015ANDA
TelmisartanTelmisartantablet, oral72241-016ANDA
TelmisartanTelmisartantablet, oral72241-017ANDA
Tizanidine hydrochlorideTizanidine hydrochloridecapsule, oral72241-041ANDA
Tizanidine hydrochlorideTizanidine hydrochloridecapsule, oral72241-042ANDA
Tizanidine hydrochlorideTizanidine hydrochloridecapsule, oral72241-043ANDA
VenlafaxineVenlafaxinetablet, coated, oral72241-075ANDA
VenlafaxineVenlafaxinetablet, coated, oral72241-076ANDA
VenlafaxineVenlafaxinetablet, coated, oral72241-077ANDA
Neighbours

Registered in the same town

3
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Comparable companies in United States

Enquiry

Common questions

Is Modavar Pharmaceuticals LLC FDA approved?
Modavar Pharmaceuticals LLC 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 Modavar Pharmaceuticals LLC's drugs manufactured?
The FDA register lists Frederick, MD. Registered operations: analytical testing, labelling, finished drug manufacture, packaging.
What drugs does Modavar Pharmaceuticals LLC make?
59 products are listed under Modavar Pharmaceuticals LLC in the openFDA NDC Directory, most often as tablet; capsule; tablet, film coated. 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.