Prednisone (Page 6 of 6)

HOW SUPPLIED

PredniSONE Tablets are available in the following strengths and package sizes:

5 mg (white, round, scored, debossed “5094” on one side and debossed “V” on the reverse side)

NDC: 70518-0305-00

PACKAGING: 21 in 1 BOX, UNIT DOSE

Dispense in a tight, light-resistant container as defined in the USP.

Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].

Repackaged and Distributed By:

Remedy Repack, Inc.

625 Kolter Dr. Suite #4 Indiana, PA 1-724-465-8762

REFERENCES

  1. Fekety R. Infections associated with corticosteroids and immunosuppressive therapy. In: Gorbach SL, Bartlett JG, Blacklow NR, eds. Infectious Diseases. Philadelphia: WBSaunders Company 1992:1050-1.
  2. Stuck AE, Minder CE, Frey FJ. Risk of infectious complications in patients taking glucocorticoids. Rev Infect Dis 1989:11(6):954-63.

Repackaged and Distributed By:

Remedy Repack, Inc.

625 Kolter Dr. Suite #4 Indiana, PA 1-724-465-8762

PRINCIPAL DISPLAY PANEL

DRUG: Prednisone

GENERIC: Prednisone

DOSAGE: TABLET

ADMINSTRATION: ORAL

NDC: 70518-0305-0

COLOR: white

SHAPE: ROUND

SCORE: Two even pieces

SIZE: 6 mm

IMPRINT: 5094;V

PACKAGING: 21 in 1 BOX, UNIT-DOSE

ACTIVE INGREDIENT(S):

  • PREDNISONE 5mg in 1

INACTIVE INGREDIENT(S):

  • SILICON DIOXIDE
  • LACTOSE MONOHYDRATE
  • MAGNESIUM STEARATE
  • STARCH, CORN
  • SODIUM STARCH GLYCOLATE TYPE A POTATO
Remedy_Label
(click image for full-size original)
PREDNISONE prednisone tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:70518-0305(NDC:0603-5337)
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
SILICON DIOXIDE
LACTOSE MONOHYDRATE
MAGNESIUM STEARATE
STARCH, CORN
SODIUM STARCH GLYCOLATE TYPE A POTATO
Product Characteristics
Color white Score 2 pieces
Shape ROUND Size 6mm
Flavor Imprint Code 5094;V
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:70518-0305-0 21 TABLET in 1 BOX, UNIT-DOSE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040256 03/10/2017
Labeler — REMEDYREPACK INC. (829572556)

Revised: 01/2021 REMEDYREPACK INC.

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