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BE Pharmaceuticals Inc.

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Registered sites
0
Active NDC listings
29
Live patents
0
Countries
0
Catalogue

Drug listings by form and route

29

29 active NDC listings: 29 human prescription drug. By marketing category: ANDA 29.

Dosage formNDCs
injection18
injection, solution6
injection, powder, lyophilized, for solution4
injection, powder, for solution1
RouteNDCs
intravenous21
subcutaneous9
intramuscular6
Labeller name on the listingNDCs
be pharmaceuticals inc.29
Catalogue

Marketed products

29
BrandGeneric nameForm / routeNDC
CARBOPROST TROMETHAMINEcarboprost tromethamineinjection, solution, intramuscular71839-137ANDA
Dalbavancindalbavancininjection, powder, lyophilized, for solution, intravenous71839-144ANDA
Heparin SodiumHeparin Sodiuminjection, solution, intravenous, subcutaneous71839-117ANDA
Heparin SodiumHeparin Sodiuminjection, solution, intravenous, subcutaneous71839-118ANDA
Neostigmine methylsulfateNeostigmine methylsulfateinjection, intravenous71839-105ANDA
Neostigmine methylsulfateNeostigmine methylsulfateinjection, intravenous71839-106ANDA
Norepinephrine Bitartratenorepinephrine bitartrateinjection, intravenous71839-143ANDA
Pantoprazole sodiumPantoprazole sodiuminjection, powder, for solution, intravenous71839-122ANDA
Phenylephrine HydrochloridePhenylephrine Hydrochlorideinjection, intravenous71839-127ANDA
Phenylephrine HydrochloridePhenylephrine Hydrochlorideinjection, intravenous71839-128ANDA
Phenylephrine HydrochloridePhenylephrine Hydrochlorideinjection, intravenous71839-129ANDA
Rocuronium Bromiderocuronium bromideinjection, solution, intravenous71839-141ANDA
Rocuronium Bromiderocuronium bromideinjection, solution, intravenous71839-142ANDA
Sodium NitroprussideSodium Nitroprussideinjection, intravenous71839-120ANDA
Succinylcholine ChlorideSuccinylcholine Chlorideinjection, solution, intramuscular, intravenous71839-121ANDA
daptomycindaptomycininjection, powder, lyophilized, for solution, intravenous71839-107ANDA
daptomycindaptomycininjection, powder, lyophilized, for solution, intravenous71839-108ANDA
enoxaparin sodiumenoxaparin sodiuminjection, subcutaneous71839-109ANDA
enoxaparin sodiumenoxaparin sodiuminjection, subcutaneous71839-110ANDA
enoxaparin sodiumenoxaparin sodiuminjection, subcutaneous71839-111ANDA
enoxaparin sodiumenoxaparin sodiuminjection, subcutaneous71839-112ANDA
enoxaparin sodiumenoxaparin sodiuminjection, subcutaneous71839-113ANDA
enoxaparin sodiumenoxaparin sodiuminjection, subcutaneous71839-115ANDA
enoxaparin sodiumenoxaparin sodiuminjection, subcutaneous71839-116ANDA
fosaprepitantfosaprepitantinjection, powder, lyophilized, for solution, intravenous71839-104ANDA
glycopyrrolateglycopyrrolateinjection, intramuscular, intravenous71839-123ANDA
glycopyrrolateglycopyrrolateinjection, intramuscular, intravenous71839-124ANDA
glycopyrrolateglycopyrrolateinjection, intramuscular, intravenous71839-125ANDA
glycopyrrolateglycopyrrolateinjection, intramuscular, intravenous71839-126ANDA
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Common questions

Is BE Pharmaceuticals Inc. FDA approved?
BE Pharmaceuticals Inc. holds no registered establishment of its own; 29 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does BE Pharmaceuticals Inc. make?
29 products are listed under BE Pharmaceuticals Inc. in the openFDA NDC Directory, most often as injection; injection, solution; injection, powder, lyophilized, for solution. 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.