Número de pieza
Desmilitarización
Vigencia
UOM
NIIN
Número de pieza:
ndc00228-2332-96
NSN
Número de acciones nacionales:
TXT
Descripción:
Usp Prednisolone Tablets
Código de nombre del artículo:
09568
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:
5.000 milligrams prednisolone active ingredient
MRC:
Those features,not otherwise specified,which may be required for proper functioning of the item.CBBL
Features Provided:
Scored
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:
A numeric value of the volume,form,or dosage within each primary container.CRLK
Primary Container Content Quantity:
1000.000 tablets
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:
The measured weight of the exterior container.ECWT
Exterior Container Weight:
48.00 pounds
MRC:
A measurement of volume taken by multiplying the length by the width by the height of the exterior container and rendered in cubic units.EXME
Exterior Container Cubic Measure:
3.00 cubic feet
MRC:
The number of units of issue placed inside the exterior container.EXQT
Exterior Container Quantity:
96
MRC:
The number of wraps,boxes,or bundles,which contains two or more units of issue,placed inside an exterior container.PKQT
Intermediate Package Quantity:
12
MRC:
A measurement of volume taken by multiplying the length by the width by the height of the unit of issue and rendered in cubic units.SUCB
Unit Of Issue Cube:
0.022 cubic feet
MRC:
The measured weight of the actual container(s) or supporting device(s) which is in direct contact with the item and its contents.SUWT
Unit Of Issue Weight:
0.70 pounds
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:
Purepac laboratories
