Potassium Chloride Extended Release (Page 3 of 3)

PRINCIPAL DISPLAY PANEL – 750 mg

Rx Only

NDC 71205-996-00

Potassium Chloride Extended-release Tablets, USP

10 mEq (750 mg)

100 Tablets

71205-996-00
(click image for full-size original)

The following image is a placeholder representing the product identifier that is either affixed or imprinted on the drug package label during the packaging operation.

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POTASSIUM CHLORIDE EXTENDED RELEASE
potassium chloride tablet, extended release
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:71205-996(NDC:0574-0275)
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
HYDROGENATED COTTONSEED OIL
SILICON DIOXIDE
MAGNESIUM STEARATE
POLYVINYL ALCOHOL, UNSPECIFIED
TITANIUM DIOXIDE
POLYETHYLENE GLYCOL, UNSPECIFIED
TALC
ALUMINUM OXIDE
D&C YELLOW NO. 10
FD&C YELLOW NO. 6
Product Characteristics
Color YELLOW Score no score
Shape ROUND Size 13mm
Flavor Imprint Code 9Q3
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71205-996-90 90 TABLET, EXTENDED RELEASE in 1 BOTTLE None
2 NDC:71205-996-00 100 TABLET, EXTENDED RELEASE in 1 BOTTLE None
3 NDC:71205-996-78 180 TABLET, EXTENDED RELEASE in 1 BOTTLE None
4 NDC:71205-996-65 270 TABLET, EXTENDED RELEASE in 1 BOTTLE None
5 NDC:71205-996-97 360 TABLET, EXTENDED RELEASE in 1 BOTTLE None
6 NDC:71205-996-55 500 TABLET, EXTENDED RELEASE in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA205993 12/11/2015
Labeler — Proficient Rx LP (079196022)
Establishment
Name Address ID/FEI Operations
Proficient Rx LP 079196022 REPACK (71205-996), RELABEL (71205-996)

Revised: 01/2020 Proficient Rx LP

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