Teilenummer
Entmilitarisierung
Lagerfähigkeit
UOM
NIIN
Teilenummer:
butisolsodium
NSN
Nationale Bestandsnummer:
TXT
Beschreibung:
Usp Butabarbital Sodium Elixir
MRC:
The ingredients compounded in a pharmaceutical preparation and recognized as having therapeutic value/s/. /usually representative in the item name generic nomenclature./AKJA
Active Medicament Medicinal Strength:
6.000 milligrams butabarbital sodium per milliliter
MRC:
The liquid nontoxic component form of a pharmacuetical preparation which normally has no therapeutic action,and presents the active ingredients to the body for absorption.AKJQ
Pharmaceutical Vehicle Type:
Aqueous
MRC:
The quality,blend,or aroma of the item that affects sense of taste.ALJH
Flavor:
Any acceptable
MRC:
Indicates the type of container/s/ or supporting device/s/ which is in direct contact with the item.CQCT
Primary Container Type:
Bottle
MRC:
Substance employed solely for the purpose of imparting color.CQJT
Err Default:
Err default
MRC:
The volume of alcohol at 15.56 degrees celsius,expressed in percent.CQLR
Err Default:
Err default
MRC:
The statements required to be included on the label of drugs subject to provisions of the federal food,drug,and cosmetic act.CQPQ
Err Default:
Err default
MRC:
A numeric value of the volume,form,or dosage within each primary container.CRLK
Primary Container Content Quantity:
1.000 gallons
MRC:
Drugs or substances subject to the provisions of the comprehensive drug abuse prevention and control act of 1970.CRYC
Controlled Substance Classification:
Schedule iii
MRC:
Represents the period beyond which the potency of the drug cannot be expected,beyond reasonable doubt,to remain effective therapeutically,or retain its required potency,expressed in months.CRYD
Err Default:
Err default
MRC:
An indication of the area,orifice,or tissue of the body to which the medication is administered or applied,based on the drug formulation.CSGS
Administration:
Oral
MRC:
An indication of the same predictable therapeutic effect as determined by the food and drug administration (fda) for an item of supply when administered under the conditions as specified in the labeling.THPE
Therapeutic Equivalent:
Any a rated drug
