Label: PREDNISONE tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 51655-320-20 - Packager: Northwind Pharmaceuticals
- This is a repackaged label.
- Source NDC Code(s): 0143-9738
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated May 1, 2014
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- Official Label (Printer Friendly)
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PRINCIPAL DISPLAY PANEL
NDC:51655-320-20
MFG: 0143-9738-10
Prednisone 20mg
20 Tablets
RX only
Dosage: See package insert
Store at 68 to 77 degrees F
Store in a tight, light-resistance container. (See USP)
Keep out of reach of children.
Each tablet contains: Prednisone, USP 20 mg
Mfg by: Hikma Pharmaceuticals Co Amman, Jordan 11118
Repackaged by Northwind Pharmaceuticals Indianapolis, IN 46256
Lot # NW46400002 Exp 07/2017
- WARNINGS AND PRECAUTIONS
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INGREDIENTS AND APPEARANCE
PREDNISONE
prednisone tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:51655-320(NDC:0143-9738) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PREDNISONE (UNII: VB0R961HZT) (PREDNISONE - UNII:VB0R961HZT) PREDNISONE 20 mg in 20 Product Characteristics Color orange Score no score Shape ROUND Size 9mm Flavor Imprint Code 477Westward Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51655-320-20 20 in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA088832 05/01/2014 Labeler - Northwind Pharmaceuticals (036986393) Registrant - Northwind Pharmaceuticals (036986393) Establishment Name Address ID/FEI Business Operations Northwind Pharmaceuticals 036986393 repack(51655-320)