Register entry

Vivus LLC

Data as of · How to read this entry

Registered sites
0
Active NDC listings
10
Labeller names
2
Live patents
24
Exclusivities
1
Countries
0
Catalogue

Drug listings by form and route

10

10 active NDC listings: 10 human prescription drug. By marketing category: BLA 6, NDA 4.

Dosage formNDCs
capsule, delayed release6
capsule, extended release4
RouteNDCs
oral10
Labeller name on the listingNDCs
vivus llc6
vivus llc4
Exclusivity

Patents and exclusivities

24
PatentProductCoversExpiry
8895057QSYMIAphentermine hydrochloride; topiramateuseJun 2028
8895058QSYMIAphentermine hydrochloride; topiramateproductJun 2028
9011905QSYMIAphentermine hydrochloride; topiramateproductJun 2028
9011906QSYMIAphentermine hydrochloride; topiramateuseJun 2028
8580298QSYMIAphentermine hydrochloride; topiramateproductMay 2029
8580299QSYMIAphentermine hydrochloride; topiramateuseJun 2029
ProductExclusivityUntil
QSYMIAPHENTERMINE HYDROCHLORIDE; TOPIRAMATEM-308 MiscellaneousSept 2027
Catalogue

Marketed products

10
BrandGeneric nameForm / routeNDC
PANCREAZEPANCRELIPASE LIPASE, PANCRELIPASE AMYLASE, and PANCRELIPASE PROTEASEcapsule, delayed release, oral62541-401BLA
PANCREAZEPANCRELIPASE LIPASE, PANCRELIPASE AMYLASE, and PANCRELIPASE PROTEASEcapsule, delayed release, oral62541-402BLA
PANCREAZEPANCRELIPASE LIPASE, PANCRELIPASE AMYLASE, and PANCRELIPASE PROTEASEcapsule, delayed release, oral62541-403BLA
PANCREAZEPANCRELIPASE LIPASE, PANCRELIPASE AMYLASE, and PANCRELIPASE PROTEASEcapsule, delayed release, oral62541-404BLA
PANCREAZEPANCRELIPASE LIPASE, PANCRELIPASE AMYLASE, and PANCRELIPASE PROTEASEcapsule, delayed release, oral62541-405BLA
PANCREAZEPANCRELIPASE LIPASE, PANCRELIPASE AMYLASE, and PANCRELIPASE PROTEASEcapsule, delayed release, oral62541-406BLA
Qsymiaphentermine and topiramatecapsule, extended release, oral62541-201NDA
Qsymiaphentermine and topiramatecapsule, extended release, oral62541-202NDA
Qsymiaphentermine and topiramatecapsule, extended release, oral62541-203NDA
Qsymiaphentermine and topiramatecapsule, extended release, oral62541-204NDA
Enquiry

Common questions

Is Vivus LLC FDA approved?
Vivus LLC holds no registered establishment of its own; 10 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does Vivus LLC make?
10 products are listed under Vivus LLC in the openFDA NDC Directory, most often as capsule, delayed release; capsule, extended 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.