NDC 50090-0152 - Furosemide

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
50090-0152
Package NDCs from labels
50090-0152-0, 50090-0152-1, 50090-0152-7, 50090-0152-8
Manufacturer
A-S Medication Solutions
Effective date
2019-03-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Furosemide - A-S Medication SolutionsA-S Medication Solutions2019-03-28HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-0152-0Furosemide30 in 1 BOTTLETABLET3013
50090-0152-1Furosemide100 in 1 BOTTLETABLET10013
50090-0152-7Furosemide200 in 1 BOTTLETABLET20013
50090-0152-8Furosemide90 in 1 BOTTLETABLET9013

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-0152FUROSEMIDE TABLET [A-S MEDICATION SOLUTIONS]134 package rows20190329_b0115c7b-48e6-4a8c-8e35-52a757cadfac.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FUROSEMIDEACTIVE INGREDIENT7LXU5N7ZO5FUROSEMIDE TABLET [A-S MEDICATION SOLUTIONS LLC]1
FUROSEMIDEACTIVE MOIETY7LXU5N7ZO5FUROSEMIDE TABLET [A-S MEDICATION SOLUTIONS LLC]1
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XFUROSEMIDE TABLET [A-S MEDICATION SOLUTIONS LLC]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30FUROSEMIDE TABLET [A-S MEDICATION SOLUTIONS LLC]1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJFUROSEMIDE TABLET [A-S MEDICATION SOLUTIONS LLC]1