رقم الجزء
تجريد
صلاحيه
UOM
NIIN
رقم الجزء:
ndc51079-0107-20
معلومات الجزء
Amitriptyline hydrochloride tablets usp 25 mg i.S. 100 per box
TXT
وصف:
Amitriptyline Hydrochloride Tabl
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:
25.000 milligrams amitriptyline hydrochloride active ingredient
MRC:
Those features,not otherwise specified,which may be required for proper functioning of the item.CBBL
Features Provided:
Individually sealed
MRC:
Indicates the type of container/s/ or supporting device/s/ which is in direct contact with the item.CQCT
Primary Container Type:
Strip
MRC:
The measured weight of the exterior container.ECWT
Exterior Container Weight:
18.00 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:
1.356 cubic feet
MRC:
The number of units of issue placed inside the exterior container.EXQT
Exterior Container Quantity:
120
MRC:
Those unusual or unique characteristics or qualities of an item not covered in the other requirements and which are determined to be essential for identification.FEAT
Special Features:
100 tablets
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:
10
MRC:
Indicates the type of container in which the item of supply is packaged.PKTY
Unit Package Type:
Package
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:
0.011 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:
0.15 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:
Any a rated drug
