Home NDC 72835-105 Syntherma Plus
Product NDC 72835-105
11-digit product format 728350105
Labeler code 72835
Product ID 72835-105_2d8d18e2-8a5d-44e1-97b4-0c2cf837bab1
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Lidocaine
Dosage form KIT
Labeler V2 Pharma, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2025-07-01
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Syntherma Plus
Listing expiration 2026-12-31 Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 415976 Internal RxNorm lookup 1745091 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 65162-791-08 Syntherma Plus 1 in 1 POUCH PATCH 30 700 mg 1 65162-791-08 Syntherma Plus 30 in 1 CARTON PATCH 700 mg 1 72667-073-01 Syntherma Plus 89 g in 1 BOTTLE, PLASTIC GEL 89 g 6 g in 100g 1 72835-105-02 Syntherma Plus 1 in 1 CARTON KIT 1 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 65162-791-08 65162079108 1 in 1 POUCH Historical 72667-073-01 72667007301 89 g in 1 BOTTLE, PLASTIC 89 g Historical 72835-105-02 72835010502 1 KIT in 1 CARTON (72835-105-02) * 30 POUCH in 1 CARTON (65162-791-08) / 1 PATCH in 1 POUCH * 89 g in 1 BOTTLE, PLASTIC (72667-073-01) 1 kit 2025-07-01 No No Current