FDA.reportPublic FDA data

NDC 50991-977 - Folite

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
50991-977
Package NDCs from labels
50991-977-30
Manufacturer
Poly Pharmaceuticals, Inc. | Formulation Technology Incorporated
Effective date
2019-08-05
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Folite - Poly Pharmaceuticals, Inc. | Formulation Technology IncorporatedPoly Pharmaceuticals, Inc. | Formulation Technology Incorporated2019-08-05DIETARY SUPPLEMENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50991-977-30Folite30 in 1 BOTTLETABLET303

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50991-977FOLITE (FOLIC ACID, MAGNESIUM CITRATE, CALCIUM CITRATE, VITAMIN D3, N-ACETYL-L-CYSTEINE) TABLET [POLY PHARMACEUTICALS, INC.]31 package rows20230331_c6589bc2-9237-414d-89dd-619725f41eab.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50991-977-30EA - Each50991-977b7abe2dd-4e87-4de1-a61f-303c7408141512019-08-06