Home NDC 71335-2970
LIDOCAINE AND PRILOCAINE
Product NDC 71335-2970
11-digit product format 713352970
Labeler code 71335
Product ID 71335-2970_f0661ee2-452d-433c-9452-bb728b9e7b7a
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Lidocaine and Prilocaine
Dosage form CREAM
Route TOPICAL
Labeler Bryant Ranch Prepack
Application ANDA212482
Marketing category ANDA
Marketing start 2022-12-20
Substance LIDOCAINE; PRILOCAINE
Active strength 25; 25 mg/g; mg/g
Pharmacologic classes Amide Local Anesthetic [EPC], Amide Local Anesthetic [EPC], Amides [CS], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE], Local Anesthesia [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base LIDOCAINE AND PRILOCAINE
Listing expiration 2026-12-31
Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE 25 mg/g PRILOCAINE 25 mg/g
Harmonized Identifiers# Field, Values table Field Values Unii 98PI200987, 046O35D44R Rxcui 197877
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71335-2970-1 LIDOCAINE AND PRILOCAINE 1 in 1 CARTON CREAM 1 100 71335-2970-1 LIDOCAINE AND PRILOCAINE 30 g in 1 TUBE CREAM 30 100
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 71335-2970-1 71335297001 1 TUBE in 1 CARTON (71335-2970-1) / 30 g in 1 TUBE 1 tube 2025-10-21 No No Current