Home NDC 0065-0245 NDC 0065-0245 - Betoptic 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 0065-0245
Package NDCs from labels 0065-0245-20, 0065-0245-05, 0065-0245-10, 0065-0245-15
Manufacturer Alcon
Effective date 2006-10-30
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Betoptic - Alcon Alcon 2006-10-30 Human Prescription Drug Label
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0065-0245-05 Betoptic 5 mL in 1 BOTTLE, PLASTIC SOLUTION/ DROPS 5 1 0065-0245-10 Betoptic 10 mL in 1 BOTTLE, PLASTIC SOLUTION/ DROPS 10 1 0065-0245-15 Betoptic 15 mL in 1 BOTTLE, PLASTIC SOLUTION/ DROPS 15 1 0065-0245-20 Betoptic 2.5 mL in 1 BOTTLE, PLASTIC SOLUTION/ DROPS 2.5 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0065-0245 BETOPTIC (BETAXOLOL HYDROCHLORIDE) SOLUTION/ DROPS [ALCON] 1 4 package rows 20080313_31b9b263-11fd-4495-83dd-ababf0d70e9e.zip
DailyMed Socrata Ingredients#