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 50 of 52 · 1,026 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
OHM Mucus Relief	ANTIMONIUM CRUDUM, ANTIMONIUM TARTARICUM, CHELIDONIUM MAJUS, FERRUM PHOSPHORICUM, KALI CARBOONICUM, KALI MURIATICUM, KALI SULPHURICUM, MARRUBIUM VULGARE.	OHM PHARMA INC.	f13bff50-7087-46dc-a958-b460a2af6283	2021-01-11	Warnings	Exact identifier unii: 660YQ98I10
POTASSIUM CHLORIDE	POTASSIUM CHLORIDE	Lupin Pharmaceuticals,Inc.	28c49165-d8c9-443a-b000-953b8e1ec55c	2020-11-20	Warnings, Adverse reactions	Exact identifier rxcui: 314182 rxcui: 312515 unii: 660YQ98I10
Lactated Ringers	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE	Asclemed USA, Inc.	afac6cc5-1ced-4639-b6f6-86f40ef5c30e	2020-10-29	Warnings, Adverse reactions	Exact identifier unii: 660YQ98I10
InterSol	PLATELET ADDITIVE 3	Fenwal, Inc.	a00c4a93-cde2-4753-81f7-0d6fee9fb690	2020-10-20	Warnings, Adverse reactions	Exact identifier unii: B22547B95K
POTASSIUM CHLORIDE IN DEXTROSE	DEXTROSE AND POTASSIUM CHLORIDE	B. Braun Medical Inc.	e5bbb3e1-ab50-4ec7-a2b4-ce4091712e23	2020-07-31	Warnings, Adverse reactions	Exact identifier unii: 660YQ98I10
Bach Original Flower Remedies	WATER	Nelson Bach USA Limited	09c76050-42c5-4403-865c-a1f6f668d9c0	2020-06-15	Warnings	Exact identifier unii: 059QF0KO0R
Cardioplegic	CALCIUM CHLORIDE, MAGNESIUM CHLORIDE, POTASSIUM CHLORIDE AND SODIUM CHLORIDE	Baxter Healthcare Corporation	1fd50ce5-2799-4c26-81da-02cf0578dd9e	2020-06-11	Warnings, Adverse reactions	Exact identifier unii: 660YQ98I10
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	ee831456-5962-4d5e-ad0c-69ab85860453	2020-06-03		Exact identifier unii: XF417D3PSL unii: B22547B95K
LACTATED RINGERS AND DEXTROSE	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE, AND DEXTROSE MONOHYDRATE	HF Acquisition Co LLC, DBA HealthFirst	a62cf623-9b8a-37e0-e053-2995a90add5b	2020-05-21	Warnings, Adverse reactions	Exact identifier unii: 660YQ98I10
Isolyte S	SODIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE, POTASSIUM CHLORIDE, AND MAGNESIUM CHLORIDE	B. Braun Medical Inc.	7e8fe27f-ff82-48c1-9bf6-3c589c8e985d	2020-05-14	Warnings, Adverse reactions	Exact identifier unii: 660YQ98I10
Potassium Chloride	POTASSIUM CHLORIDE	Genus Lifesciences Inc.	23d818e7-c076-40de-8dc1-0b51ba4be96a	2020-04-28	Warnings, Adverse reactions	Exact identifier unii: 660YQ98I10
Potassium Chloride	POTASSIUM CHLORIDE	Lupin Pharmaceuticals,Inc.	1bbacdbb-91fa-4897-a00c-1b293de27b83	2020-04-27	Warnings, Adverse reactions	Exact identifier unii: 660YQ98I10
Potassium Chloride	POTASSIUM CHLORIDE	Mylan Pharmaceuticals Inc.	c64ed4c0-1e27-42b3-9625-fb4e0d31e271	2020-04-15	Warnings, Adverse reactions	Exact identifier unii: 660YQ98I10
Dextrose and Electrolyte No. 48	SODIUM LACTATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, MONOBASIC POTASSIUM PHOSPHATE, SODIUM CHLORIDE AND DEXTROSE MONOHYDRATE	Baxter Healthcare Company	b283a454-0c20-4fbf-92d3-dae1f3cd3cad	2020-02-13	Warnings, Adverse reactions	Exact identifier unii: 660YQ98I10
Sterile Water	WATER	Baxter Healthcare Company	8bcf5572-49e1-4302-9522-56f57904cb4a	2019-12-29	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Renacidin	CITRIC ACID, GLUCONOLACTONE AND MAGNESIUM CARBONATE	United-Guardian, Inc.	13a9bbba-db21-4cba-991c-5d8afaf2ed74	2019-12-17	Warnings, Adverse reactions	Exact identifier unii: XF417D3PSL
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	e41adb4e-06fb-4141-ba55-50b043f3c9da	2019-11-19		Exact identifier unii: XF417D3PSL unii: B22547B95K
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	14445dfd-6041-40cd-a043-3f4da6bcb9c1	2019-11-18		Exact identifier unii: XF417D3PSL unii: B22547B95K
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	2557199a-5f60-49d8-b093-1e0700211243	2019-11-18		Exact identifier unii: XF417D3PSL unii: B22547B95K
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	794f724c-87f0-49c1-9b26-c9e491978313	2019-11-18		Exact identifier unii: XF417D3PSL unii: B22547B95K

Reported adverse events (FAERS/openFDA)#

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