NDC 50480-010 - Keto-Plex Forte

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: 50480-010
Package NDCs from labels: 50480-010-99
Manufacturer: Radix Laboratories, Inc.
Effective date: 2014-12-22
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
KETO-PLEX FORTE	Radix Laboratories, Inc.	2014-12-22	OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
50480-010-99	Keto-Plex Forte	12 in 1 CARTON	LIQUID	12		3
50480-010-99	Keto-Plex Forte	1000 mL in 1 BOTTLE, PLASTIC	LIQUID	1000		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50480-010	KETO-PLEX FORTE LIQUID [RADIX LABORATORIES, INC.]	3	2 package rows	20141222_9ffb3492-408b-401e-a507-ae059f47e053.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
AMINO ACIDS	ACTIVE INGREDIENT	0O72R8RF8A	KETO-PLEX FORTE LIQUID [RADIX LABORATORIES, INC.]	3
CALCIUM CHLORIDE	ACTIVE INGREDIENT	M4I0D6VV5M	KETO-PLEX FORTE LIQUID [RADIX LABORATORIES, INC.]	3
DEXTROSE MONOHYDRATE	ACTIVE INGREDIENT	LX22YL083G	KETO-PLEX FORTE LIQUID [RADIX LABORATORIES, INC.]	3
MAGNESIUM CHLORIDE	ACTIVE INGREDIENT	02F3473H9O	KETO-PLEX FORTE LIQUID [RADIX LABORATORIES, INC.]	3
AMINO ACIDS	ACTIVE MOIETY	0O72R8RF8A	KETO-PLEX FORTE LIQUID [RADIX LABORATORIES, INC.]	3
ANHYDROUS DEXTROSE	ACTIVE MOIETY	5SL0G7R0OK	KETO-PLEX FORTE LIQUID [RADIX LABORATORIES, INC.]	3
CALCIUM CATION	ACTIVE MOIETY	2M83C4R6ZB	KETO-PLEX FORTE LIQUID [RADIX LABORATORIES, INC.]	3
MAGNESIUM CATION	ACTIVE MOIETY	T6V3LHY838	KETO-PLEX FORTE LIQUID [RADIX LABORATORIES, INC.]	3

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 13 of 13 · 245 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Potassium Chloride in Dextrose and Sodium Chloride	POTASSIUM CHLORIDE, DEXTROSE MONOHYDRATE AND SODIUM CHLORIDE	Baxter Healthcare Company	c553fed1-3de5-4826-8eff-633b5923bf0b	2019-02-21	Warnings, Adverse reactions	Exact identifier unii: LX22YL083G
Lactated Ringers	SODIUM CHLORIDE, SOLDIUM LACTATE, POTASSIUM CHLORIDE AND CALCIUM CHLORIDE	Baxter Healthcare Company	5215ec33-8cfe-4885-ae92-e6a12100bd27	2018-01-02	Warnings, Adverse reactions	Exact identifier unii: M4I0D6VV5M
CPDA-1	ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE	Fenwal, Inc.	051f7347-5a76-4664-8fe2-e61b3dfcb0e4	2014-08-27		Exact identifier unii: LX22YL083G
Ringers	SODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE,	Baxter Healthcare Corporation	e1953d54-818d-46a6-8532-518ebae6d84e	2012-06-13		Exact identifier unii: M4I0D6VV5M
Lactated Ringers	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE	Baxter Healthcare Corporation	f09f80bf-2f8b-4420-865d-aec2d5e5cd4d	2012-06-12		Exact identifier unii: M4I0D6VV5M

Reported adverse events (FAERS/openFDA)#

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