Potassium Chloride (Page 3 of 3)

HOW SUPPLIED

Potassium Chloride Extended Release Tablets, USP 20 mEq are available in bottles of 100 (NDC 0085-1718-02) and 1000 (NDC 0085-1718-01). Potassium Chloride Extended Release Tablets, USP 20 mEq are white to off-white capsule-shaped tablets imprinted “W-1714″ and scored on the other side.

Potassium Chloride Extended Release Tablets, USP 10 mEq are available in bottles of 100 (NDC 0085-1717-01). Potassium Chloride Extended Release Tablets, USP 10 mEq are white to off-white capsule-shaped tablets imprinted “W-1715″ on one side and plain on the other side.

Storage Conditions

Keep tightly closed. Store at 25°C (77°F); excursions permitted to 15°–30°C (59°–86°F) [see USP Controlled Room Temperature]

Rx only.

Schering Corporation Kenilworth, NJ 07033 USA

Copyright © 1986, 2006, Schering Corporation. All rights reserved.

Rev. 3/08

PRINCIPAL DISPLAY PANEL — 100 20 mEq K Tablet Bottle Label

NDC 0085-1718 -02

100 Tablets

Potassium Chloride
Extended Release Tablets USP

20 mEq K

Rx only

Each extended release
tablet provides 1500 mg KCl

Schering-Plough

PRINCIPAL DISPLAY PANEL -- 100 20 mEq Tablet Bottle Label
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 100 10 mEq K Tablet Bottle Label

NDC 0085-1717 -01

100 Tablets

Potassium Chloride
Extended Release Tablets USP

10 mEq K

Rx only

Each extended release
tablet provides 750 mg KCl

Schering-Plough

PRINCIPAL DISPLAY PANEL -- 100 10 mEq Tablet Bottle Label
(click image for full-size original)
POTASSIUM CHLORIDE
potassium chloride tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0085-1718
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Potassium Chloride (Potassium cation) Potassium Chloride 1500 mg
Inactive Ingredients
Ingredient Name Strength
Crospovidone
Ethylcelluloses
Hydroxypropyl Cellulose (Type H)
Magnesium Stearate
Cellulose, Microcrystalline
Product Characteristics
Color WHITE (White to Off-White) Score 2 pieces
Shape OVAL (Capsule shaped) Size 20mm
Flavor Imprint Code W;1714
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0085-1718-02 100 TABLET, EXTENDED RELEASE in 1 BOTTLE None
2 NDC:0085-1718-01 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA019439 06/13/1986
POTASSIUM CHLORIDE
potassium chloride tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0085-1717
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Potassium Chloride (Potassium Cation) Potassium Chloride 750 mg
Inactive Ingredients
Ingredient Name Strength
Crospovidone
Ethylcelluloses
Hydroxypropyl Cellulose (Type H)
Magnesium Stearate
Cellulose, Microcrystalline
Product Characteristics
Color WHITE (White to Off-White) Score no score
Shape OVAL (Capsule shaped) Size 15mm
Flavor Imprint Code W;1715
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0085-1717-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA019439 06/13/1986
Labeler — Merck Sharp & Dohme Corp. (001317601)
Establishment
Name Address ID/FEI Operations
Schering Plough Products LLC 606266625 MANUFACTURE (0085-1718) (0085-1717)
Establishment
Name Address ID/FEI Operations
MALLINCKRODT, INC. 163205300 API MANUFACTURE (0085-1718) (0085-1717)

Revised: 06/2008 Merck Sharp & Dohme Corp.

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