NDC 58768-735 - Carbastat

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: 58768-735
Package NDCs from labels: 58768-735-12
Manufacturer: Novartis Ophthalmics
Effective date: 2006-09-19
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Carbastat - Novartis Ophthalmics	Novartis Ophthalmics	2006-09-19	HUMAN PRESCRIPTION DRUG LABELING

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Carbachol	ACTIVE INGREDIENT	8Y164V895Y	CARBASTAT (CARBACHOL) INJECTION, SOLUTION [NOVARTIS OPHTHALMICS]	1
Carbachol	ACTIVE MOIETY	8Y164V895Y	CARBASTAT (CARBACHOL) INJECTION, SOLUTION [NOVARTIS OPHTHALMICS]	1
calcium chloride dihydrate	INACTIVE INGREDIENT	M4I0D6VV5M	CARBASTAT (CARBACHOL) INJECTION, SOLUTION [NOVARTIS OPHTHALMICS]	1
hydrochloric acid	INACTIVE INGREDIENT	QTT17582CB	CARBASTAT (CARBACHOL) INJECTION, SOLUTION [NOVARTIS OPHTHALMICS]	1
magnesium chloride hexahydrate	INACTIVE INGREDIENT	02F3473H9O	CARBASTAT (CARBACHOL) INJECTION, SOLUTION [NOVARTIS OPHTHALMICS]	1
potassium chloride	INACTIVE INGREDIENT	660YQ98I10	CARBASTAT (CARBACHOL) INJECTION, SOLUTION [NOVARTIS OPHTHALMICS]	1
sodium acetate trihydrate	INACTIVE INGREDIENT	4550K0SC9B	CARBASTAT (CARBACHOL) INJECTION, SOLUTION [NOVARTIS OPHTHALMICS]	1
Sodium chloride	INACTIVE INGREDIENT	451W47IQ8X	CARBASTAT (CARBACHOL) INJECTION, SOLUTION [NOVARTIS OPHTHALMICS]	1
sodium citrate dihydrate	INACTIVE INGREDIENT	B22547B95K	CARBASTAT (CARBACHOL) INJECTION, SOLUTION [NOVARTIS OPHTHALMICS]	1
sodium hydroxide	INACTIVE INGREDIENT	55X04QC32I	CARBASTAT (CARBACHOL) INJECTION, SOLUTION [NOVARTIS OPHTHALMICS]	1
water	INACTIVE INGREDIENT	059QF0KO0R	CARBASTAT (CARBACHOL) INJECTION, SOLUTION [NOVARTIS OPHTHALMICS]	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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
048AF9C6-4866-4500-9914-CD7071A19B63			048AF9C6-4866-4500-9914-CD7071A19B63	2006-09-19	Warnings, Adverse reactions	Exact identifier spl id: 048AF9C6-4866-4500-9914-CD7071A19B63 spl set id: 048AF9C6-4866-4500-9914-CD7071A19B63

Reported adverse events (FAERS/openFDA)#

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