NDC 57932-004 - MUCUSOL

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
57932-004
Package NDCs from labels
57932-004-33, 57932-004-85
Manufacturer
Animal Science Products Inc
Effective date
2025-10-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
MUCUSOL - Animal Science Products IncAnimal Science Products Inc2025-10-28OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57932-004-33MUCUSOL1 L in 1 BOTTLE, PLASTICLIQUID18
57932-004-33MUCUSOL12 in 1 BOXLIQUID128
57932-004-85MUCUSOL4 in 1 BOXLIQUID48
57932-004-85MUCUSOL3.785 L in 1 BOTTLE, PLASTICLIQUID3.7858

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57932-004MUCUSOL (GUAIFENESIN) LIQUID [ANIMAL SCIENCE PRODUCTS INC]74 package rows20241120_9a3f534c-3bfb-47d4-ac40-6f30023b7609.zip