Register entry

H2-Pharma, LLC

Registered sites
0
Drug products
48
Live patents
0
Countries
0
Base
Unknown
Sites

Facilities

0

No registered facilities

This company holds drug listings or approvals but operates no registered establishment of its own, which is normal for an NDA holder that outsources manufacturing.

Catalogue

Marketed products

48

Showing 48 of 48.

BrandGeneric nameFormCategory
Bismuth Subcitrate Potassium, Metronidazole and Tetracycline HydrochlorideBismuth Subcitrate Potassium, Metronidazole and Tetracycline HydrochlorideCAPSULENDA AUTHORIZED GENERIC
Childrens Allergyfexofenadine hydrochlorideSUSPENSIONANDA
ClotrimazoleClotrimazoleCREAMANDA
DOCOSANOLDOCOSANOLCREAMANDA
DOCOSANOLDOCOSANOLCREAMANDA
DROXIAHYDROXYUREACAPSULENDA
DROXIAHYDROXYUREACAPSULENDA
DROXIAHYDROXYUREACAPSULENDA
ETOPOPHOSetoposide phosphateINJECTION, POWDER, LYOPHILIZED, FOR SOLUTIONNDA
HYDREAHYDROXYUREACAPSULENDA
KlonopinClonazepamTABLETNDA
KlonopinClonazepamTABLETNDA
KlonopinClonazepamTABLETNDA
Miconazole 7Miconazole NitrateCREAMANDA
ORLISTATorlistatCAPSULENDA AUTHORIZED GENERIC
PULMICORT FLEXHALERBudesonideAEROSOL, POWDERNDA
PULMICORT FLEXHALERBudesonideAEROSOL, POWDERNDA
PYLERABISMUTH SUBCITRATE POTASSIUM, METRONIDAZOLE, and TETRACYCLINE HYDROCHLORIDECAPSULENDA
PYLERABISMUTH SUBCITRATE POTASSIUM, METRONIDAZOLE, AND TETRACYCLINE HYDROCHLORIDECAPSULENDA
SEROQUELquetiapineTABLET, FILM COATEDNDA
SEROQUELquetiapineTABLET, FILM COATEDNDA
SEROQUELquetiapineTABLET, FILM COATEDNDA
SEROQUELquetiapineTABLET, FILM COATEDNDA
SEROQUELquetiapineTABLET, FILM COATEDNDA
SEROQUELquetiapineTABLET, FILM COATEDNDA
SEROQUEL XRquetiapineTABLET, EXTENDED RELEASENDA
SEROQUEL XRquetiapineTABLET, EXTENDED RELEASENDA
SEROQUEL XRquetiapineTABLET, EXTENDED RELEASENDA
SEROQUEL XRquetiapineTABLET, EXTENDED RELEASENDA
SEROQUEL XRquetiapineTABLET, EXTENDED RELEASENDA
ValcytevalganciclovirTABLET, FILM COATEDNDA
Valcytevalganciclovir hydrochloridePOWDER, FOR SOLUTIONNDA
XELODAcapecitabineTABLET, FILM COATEDNDA
XenicalorlistatCAPSULENDA
ZYPREXA IntramuscularOlanzapineINJECTION, POWDER, FOR SOLUTIONNDA
ZYPREXA RelprevvOlanzapine pamoateKITNDA
ZYPREXA RelprevvOlanzapine pamoateKITNDA
ZYPREXA RelprevvOlanzapine pamoateKITNDA
ZYPREXA ZydisOlanzapineTABLET, ORALLY DISINTEGRATINGNDA
ZYPREXA ZydisOlanzapineTABLET, ORALLY DISINTEGRATINGNDA
ZYPREXA ZydisOlanzapineTABLET, ORALLY DISINTEGRATINGNDA
ZYPREXA ZydisOlanzapineTABLET, ORALLY DISINTEGRATINGNDA
ZyprexaOlanzapineTABLETNDA
ZyprexaOlanzapineTABLETNDA
ZyprexaOlanzapineTABLETNDA
ZyprexaOlanzapineTABLETNDA
ZyprexaOlanzapineTABLETNDA
ZyprexaOlanzapineTABLETNDA
Provenance

Facility and operations data from the FDA Drug Establishments Current Registration Site. Product data from the openFDA National Drug Code Directory. Patent and exclusivity data from the FDA Orange Book. Shortage data from the FDA drug shortage database. Contact details the FDA publishes for registered establishments are deliberately not reproduced here. This entry is compiled from public records and has not been claimed by the company.