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SUBCUTANEOUS ROUTE
INTRADERMAL ROUTE
ID INJECTIO N OF IMMUNIZ ATON SUBSTA NCE
DIFFERENCES BETWEEN PARENTERALS AND OTHER DOSAGE FORM SOLVENTS OR VEHICLE MUST MEET
SPECIAL PURITY USE OF ADDED SUBSTANCES FALLS UNDER SPECIFIC GUIDELINES OF USE AND RESTRICTED IN CERTAIN PARENTERAL PRODUCTS. USE OF COLORING AGENTS IS STRICTLY PROHITED SHOULD MEET STERILITY STANDARDS AND MUST BE PYROGEN LIMITED MUST MEET COMPENDIAL STANDARDS FOR
DIFFERENCES BETWEEN PARENTERALS AND OTHER DOSAGE FORM EACH CONTAINER OF AN INJECTION
IS FILLED TO VOLUME IN SLIGHT EXCESS OF THE LABELED TO BE WITHDRAWN. VOLUME OF INJECTION PERMITTED IN MULTIPLE CONTAINERS ARE RESTRICTED AS ARE TYPES OF CONTAINERS THAT MAY BE USED FOR CERTAIN INJECTIONS. SPECIFIC LABELING REGULATIONS APPLY TO INJECTIONS
NMT 1 mg/100 mL WATER FOR INJECTION MUST BE PYROGEN FREE INTENDED FOR MANUFACTURING INJECTABLE PRODUCTS TO BE STERILIZED AFTER PREPARATIONS STORED IN TIGHT CONTAINERS SHOULD BE USED WITHIN 24 HOURS AFTER COLLECTION CONTAINERS ARE USUALLY GLASS OR GLASS LINED
SOLVENTS AND VEHICLES FOR INJECTIONS STERILE WATER FOR INJECTION, USP
PACKAGED IN SINGLE DOSE NLT 1L PYROGEN FREE AND NMT .25 USP ENDOTOXIN / Ml NO ANTIMICROBIAL AGENT OR OTHER ADDED SUBSTANCE INTENDED TO BE USED AS A SOLVENT, VEHICLE OR DILUENT 1L BOTTLES CANNOT BE ADMINISTERED IV
USED AS RECONSTITUTION OF MULTIPLE ANTIBIOTICS
EMPLOYED AS A VEHICLE FOR DRUGS ACTS AS AN ELECTROLYTE REPLENISHER AND PLASMA VOLUME EXPANDER