Prednisone (Page 4 of 4)

PRINCIPAL PANEL DISPLAY- 10 mg 100s

Label Graphic -- 10 mg 100s
(click image for full-size original)

PRINCIPAL PANEL DISPLAY- 20 mg 100s

Label Graphic -- 20 mg 100s
(click image for full-size original)
PREDNISONE prednisone tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:60429-130(NDC:0143-1475)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PREDNISONE (PREDNISONE) PREDNISONE 5 mg
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS LACTOSE
COLLOIDAL SILICON DIOXIDE
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
SODIUM STARCH GLYCOLATE TYPE A POTATO
TALC
Product Characteristics
Color WHITE Score 2 pieces
Shape ROUND (debossed) Size 6mm
Flavor Imprint Code Westward;475
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:60429-130-01 100 TABLET in 1 BOTTLE None
2 NDC:60429-130-10 1000 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA080292 08/03/2009
PREDNISONE prednisone tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:60429-131(NDC:0143-1473)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PREDNISONE (PREDNISONE) PREDNISONE 10 mg
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS LACTOSE
COLLOIDAL SILICON DIOXIDE
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
SODIUM STARCH GLYCOLATE TYPE A POTATO
TALC
Product Characteristics
Color WHITE Score 2 pieces
Shape ROUND (debossed) Size 9mm
Flavor Imprint Code Westward;473
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:60429-131-01 100 TABLET in 1 BOTTLE None
2 NDC:60429-131-05 500 TABLET in 1 BOTTLE None
3 NDC:60429-131-10 1000 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA088832 08/03/2009
PREDNISONE prednisone tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:60429-132(NDC:0143-1477)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PREDNISONE (PREDNISONE) PREDNISONE 20 mg
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS LACTOSE
D&C YELLOW NO. 10
FD&C YELLOW NO. 6
MAGNESIUM STEARATE
CELLULOSE, MICROCRYSTALLINE
SODIUM STARCH GLYCOLATE TYPE A POTATO
Product Characteristics
Color ORANGE (Peach) Score 2 pieces
Shape ROUND Size 9mm
Flavor Imprint Code Westward;477
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:60429-132-01 100 TABLET in 1 BOTTLE None
2 NDC:60429-132-05 500 TABLET in 1 BOTTLE None
3 NDC:60429-132-10 1000 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA083677 08/03/2009
Labeler — Golden State Medical Supply, Inc. (603184490)
Establishment
Name Address ID/FEI Operations
Golden State Medical Supply, Inc. 603184490 REPACK (60429-130), REPACK (60429-131), REPACK (60429-132), RELABEL (60429-130), RELABEL (60429-131), RELABEL (60429-132)

Revised: 01/2012 Golden State Medical Supply, Inc.

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