Prednisone (Page 3 of 3)

HOW SUPPLIED

NDC: 71335-2122-2: 54 TABLETs in a BOTTLE

NDC: 71335-2122-3: 90 TABLETs in a BOTTLE

NDC: 71335-2122-1: 5 TABLETs in a BOTTLE

PredniSONE 10mg Tablet

Label
(click image for full-size original)
PREDNISONE
prednisone tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:71335-2122(NDC:64380-784)
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
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
STARCH, CORN
SODIUM STARCH GLYCOLATE TYPE A POTATO
Product Characteristics
Color WHITE Score 2 pieces
Shape ROUND Size 7mm
Flavor Imprint Code P10
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71335-2122-2 54 TABLET in 1 BOTTLE None
2 NDC:71335-2122-3 90 TABLET in 1 BOTTLE None
3 NDC:71335-2122-1 5 TABLET in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA208412 09/01/2021
Labeler — Bryant Ranch Prepack (171714327)
Registrant — Bryant Ranch Prepack (171714327)
Establishment
Name Address ID/FEI Operations
Bryant Ranch Prepack 171714327 REPACK (71335-2122), RELABEL (71335-2122)

Revised: 06/2022 Bryant Ranch Prepack

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