Active Ingredient History
Dicloxacillin sodium USP is a semisynthetic antibiotic substance which resists destruction by the enzyme penicillinase (beta-lactamase). It is monosodium (2S,5R,6R)-6-[3-(2,6-dichlorophenyl)-5-methyl-4- isoxazolecarboxamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo [3.2.0]heptane-2-carboxylate monohydrate. Like other β-lactam antibiotics, dicloxacillin acts by inhibiting the synthesis of bacterial cell walls. It inhibits cross-linkage between the linear peptidoglycan polymer chains that make up a major component of the cell wall of Gram-positive bacteria. Dicloxacillin is administered orally via capsule form or powder for reconstitution. NCATS
Drug Pricing (per unit)
Note: This drug pricing data is preliminary, incomplete, and may contain errors.
Organization | Org Type | FDA approvals | Clinical Trials involvement | Org ID | Force Sort |
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Organization | Org Type | FDA approvals | Clinical Trials involvement | Org ID | Force Sort |
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Arthritis, Infectious (Phase 4)
Bacteremia (Phase 4)
Bacterial Infections (Phase 3)
Bone Diseases, Infectious (Phase 4)
Dermatitis, Atopic (Phase 4)
Drug Interactions (Phase 1)
Eczema (Phase 4)
Endocarditis (Phase 4)
Gram-Positive Bacterial Infections (Phase 3)
Healthy Volunteers (Phase 1)
Infections (Phase 4)
Osteomyelitis (Phase 4)
Trial | Phase | Start Date | Organizations | Indications |
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