NDC 66689-047-01 - Potassium Chloride

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 66689-047
Requested NDC: 66689-047-01
Package NDCs from labels: 66689-047-01, 66689-047-50, 66689-047-99, 66689-047-30, 66689-047-80
Manufacturer: VistaPharm, LLC
Effective date: 2024-05-09
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Potassium Chloride - VistaPharm, LLC	VistaPharm, LLC	2024-05-09	HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDC	Related label
66689-047-30	These highlights do not include all the information needed to use POTASSIUM CHLORIDE safely and effectively. See full prescribing information for POTASSIUM CHLORIDE. POTASSIUM CHLORIDE oral solution Initial U.S. Approval: 1948
66689-047-50	These highlights do not include all the information needed to use POTASSIUM CHLORIDE safely and effectively. See full prescribing information for POTASSIUM CHLORIDE. POTASSIUM CHLORIDE oral solution Initial U.S. Approval: 1948
66689-047-80	These highlights do not include all the information needed to use POTASSIUM CHLORIDE safely and effectively. See full prescribing information for POTASSIUM CHLORIDE. POTASSIUM CHLORIDE oral solution Initial U.S. Approval: 1948
66689-047-99	These highlights do not include all the information needed to use POTASSIUM CHLORIDE safely and effectively. See full prescribing information for POTASSIUM CHLORIDE. POTASSIUM CHLORIDE oral solution Initial U.S. Approval: 1948

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
66689-047	POTASSIUM CHLORIDE SOLUTION [VISTAPHARM, LLC]	15	Legacy NDC	20240511_142c30ff-a839-4616-8167-ad4b07d8456f.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
66689-047-01	ML - Milliliter	66689-047	bb1736ab-dff9-425e-96b9-0b14a2b2da91	1	2016-03-04
66689-047-30	ML - Milliliter	66689-047	9bfe89f8-8f34-4cb6-b8f3-2a4a4e298b60	1	2017-07-07
66689-047-50	ML - Milliliter	66689-047	dcc36d0c-834f-4de0-b82b-51b62fc79b12	1	2016-03-04
66689-047-80	ML - Milliliter	66689-047	729fbfda-64b8-4c88-ae26-404d0df09f64	1	2017-07-07

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Potassium Chloride	ACTIVE INGREDIENT	660YQ98I10	POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]	1
Chloride Ion	ACTIVE MOIETY	Q32ZN48698	POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]	1
Anhydrous Citric Acid	INACTIVE INGREDIENT	XF417D3PSL	POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]	1
FD&C Yellow NO. 6	INACTIVE INGREDIENT	H77VEI93A8	POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]	1
Glycerin	INACTIVE INGREDIENT	PDC6A3C0OX	POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]	1
Methylparaben	INACTIVE INGREDIENT	A2I8C7HI9T	POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]	1
Propylene Glycol	INACTIVE INGREDIENT	6DC9Q167V3	POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]	1
Propylparaben	INACTIVE INGREDIENT	Z8IX2SC1OH	POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]	1
Sucralose	INACTIVE INGREDIENT	96K6UQ3ZD4	POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]	1
Trisodium Citrate Dihydrate	INACTIVE INGREDIENT	B22547B95K	POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]	1
Water	INACTIVE INGREDIENT	059QF0KO0R	POTASSIUM CHLORIDE SOLUTION [VISTAPHARM INC.]	1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 52 of 52 · 1,026 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Eye Wash	WATER	CVS Pharmacy	049cee29-7ec2-4d5b-8308-f522acde43a7	2017-03-29	Warnings	Exact identifier unii: 059QF0KO0R
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	051f7347-5a76-4664-8fe2-e61b3dfcb0e4	2014-08-27		Exact identifier unii: XF417D3PSL unii: B22547B95K
TIS-U-SOL	SODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATE	Baxter Healthcare Corporation	9da4121f-d62d-4da4-8dfb-0494da16015f	2014-02-21		Exact identifier unii: 660YQ98I10
Ringers	SODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE,	Baxter Healthcare Corporation	e1953d54-818d-46a6-8532-518ebae6d84e	2012-06-13		Exact identifier unii: 660YQ98I10
Lactated Ringers	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE	Baxter Healthcare Corporation	f09f80bf-2f8b-4420-865d-aec2d5e5cd4d	2012-06-12		Exact identifier unii: 660YQ98I10

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.