NDC 81266-920

DIBUCAINE

Dibucaine

DIBUCAINE is a Topical Ointment in the Human Otc Drug category. It is labeled and distributed by Nugeri Llc. The primary component is Dibucaine.

Product ID81266-920_b6ca4519-6c8f-49e0-e053-2995a90af800
NDC81266-920
Product TypeHuman Otc Drug
Proprietary NameDIBUCAINE
Generic NameDibucaine
Dosage FormOintment
Route of AdministrationTOPICAL
Marketing Start Date2021-05-01
Marketing CategoryOTC MONOGRAPH FINAL /
Application Numberpart346
Labeler NameNUGERI LLC
Substance NameDIBUCAINE
Active Ingredient Strength0 g/g
Pharm ClassesAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 81266-920-01

28 g in 1 TUBE (81266-920-01)
Marketing Start Date2021-05-01
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "DIBUCAINE" or generic name "Dibucaine"

NDCBrand NameGeneric Name
0168-0046DIBUCAINEDIBUCAINE
45802-050dibucainedibucaine
54162-011DibucaineDibucaine
57896-131DibucaineDibucaine 1%
59779-398DIBUCAINEDIBUCAINE
63868-911DibucaineDibucaine 1%
69396-023DibucaineDibucaine 1%
71399-2829DibucaineDibucaine
81266-920DIBUCAINEDIBUCAINE
59779-997CVS Hemorrhoidal Topical AnalgesicDibucaine
0536-1211Dibucaine Topical Anesthetic 1% HemorrhoidalDIBUCAINE
55741-402NupercainalDibucaine

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.