FDA.reportPublic FDA data

Converthera NAD plus Patch

Product NDC
85945-0001
11-digit product format
859450001
Labeler code
85945
Product ID
85945-0001_3a33f86a-c86c-9023-e063-6394a90a0f39
Type
HUMAN OTC DRUG
Nonproprietary name
Converthera NAD plus Patch
Dosage form
PATCH
Route
TRANSDERMAL
Labeler
Through Medical INC.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2025-07-01
Substance
GLUTATHIONE; NICOTINAMIDE ADENINE DINUCLEOTIDE
Active strength
25; 250 mg/U; mg/U
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 3 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct85945-0001IInactivated by FDA2026-08-07
excluded packagepackage85945-000185945-0001-1IInactivated by FDA2026-08-07
excluded packagepackage85945-000185945-0001-2IInactivated by FDA2026-08-07

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85945-0001-1Converthera NAD plus Patch30 U in 1 PATCHPATCH301
85945-0001-2Converthera NAD plus Patch8 U in 1 PATCHPATCH81

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85945-0001-18594500010130 U in 1 PATCH (85945-0001-1) 30 u2025-07-01NoNoHistorical
85945-0001-2859450001028 U in 1 PATCH (85945-0001-2) 8 u2025-07-01NoNoHistorical