FDA.reportPublic FDA data

NDC 68001-702 - Labetalol Hydrochloride

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
68001-702
Package NDCs from labels
68001-702-00, 68001-702-03
Manufacturer
BluePoint Laboratories | Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.
Effective date
2026-06-04
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Labetalol Hydrochloride Tablets, USP Rx onlyBluePoint Laboratories | Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.2026-06-04HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68001-702-00Labetalol Hydrochloride100 in 1 BOTTLETABLET1002
68001-702-03Labetalol Hydrochloride500 in 1 BOTTLETABLET5002