NDC 57664-997 - Metformin 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
57664-997
Package NDCs from labels
57664-997-99, 57664-997-88, 57664-997-13, 57664-997-18
Manufacturer
CARACO PHARMACEUTICAL LABORATORIES, LTD.
Effective date
2008-09-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Metformin Hydrochloride - CARACO PHARMACEUTICAL LABORATORIES, LTD.CARACO PHARMACEUTICAL LABORATORIES, LTD.2008-09-16HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57664-997-13Metformin Hydrochloride500 in 1 BOTTLETABLET, EXTENDED RELEASE5002
57664-997-18Metformin Hydrochloride1000 in 1 BOTTLETABLET, EXTENDED RELEASE10002
57664-997-88Metformin Hydrochloride100 in 1 BOTTLETABLET, EXTENDED RELEASE1002
57664-997-99Metformin Hydrochloride90 in 1 BOTTLETABLET, EXTENDED RELEASE902

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57664-997METFORMIN HYDROCHLORIDE TABLET, EXTENDED RELEASE [CARACO PHARMACEUTICAL LABORATORIES, LTD.]24 package rows20081114_542c7f49-abdc-4937-bca2-f51c553c5286.zip

DailyMed Socrata Ingredients#