Oxacilina

Bactocill

10GM BASE/VIAL, 1GM BASE/VIAL, 2GM BASE/VIAL injectableVereinigte StaatenNicht im HandelZugelassen am 26. März 1982

In anderen Ländern

Dieselben Wirkstoffe in anderen Registern, dieselbe Marke zuerst.

OXACILINA ATB 1000 mgRumänien · 1000mg · pulb. pt. sol. inj./perf. · Antibiotice SAGleiche Darreichungsform
OXACILINA ATB 1000mgRumänien · 1000mg · pulb. pt. sol. inj./perf. · Antibiotice SAGleiche Darreichungsform
OXACILINA ATB 1gRumänien · 1g · pulb. pt. sol. inj. / perf. · Antibiotice SAGleiche Darreichungsform
OxacililBrasilien · Newcom Farmaceutica Ltda.Gleicher Wirkstoff
oxacilina sódicaBrasilien · Blau Farmacêutica S.A.Gleicher Wirkstoff
Oxacilina SodicaBrasilien · Laboratório Teuto Brasileiro S/AGleicher Wirkstoff
Oxacillin Powder for Injection "CYH"Taiwan · 乾粉注射劑 · 中化裕民健康事業股份有限公司Gleicher Wirkstoff

Packung	Code	Status
OXACILLIN SODIUM EQ 500MG BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ANDA061334-009	Discontinued
OXACILLIN SODIUM EQ 2GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ANDA061334-007	Discontinued
OXACILLIN SODIUM EQ 4GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ANDA061334-008	Discontinued
OXACILLIN SODIUM EQ 1GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ANDA061334-006	Discontinued
OXACILLIN SODIUM EQ 10GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ANDA061334-010	Discontinued
OXACILLIN SODIUM EQ 1GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ANDA062736-001	Discontinued
OXACILLIN SODIUM EQ 2GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	ANDA062736-002	Discontinued