NDC 63304-202 - Nortriptyline 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
63304-202
Package NDCs from labels
63304-202-01
Manufacturer
Ranbaxy Laboratories Limited
Effective date
2008-01-04
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Nortriptyline Hydrochloride - Ranbaxy Laboratories LimitedRanbaxy Laboratories Limited2008-01-04HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63304-202-01Nortriptyline Hydrochloride480 mL in 1 BOTTLESOLUTION4801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63304-202NORTRIPTYLINE HYDROCHLORIDE (NORTRIPTYLINE HYDROCHLORIDE) SOLUTION [RANBAXY LABORATORIES LIMITED]11 package rows20080111_ced93eb0-e8b6-44b8-9d2c-e2afa92500f7.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63304-202-01ML - Milliliter63304-20215aaeefe-0d59-4cfe-8885-0d0debe8053112013-02-13

DailyMed Socrata Ingredients#