DIBUCAINE - 0168-0046-31 - (DIBUCAINE)

Alphabetical Index


Drug Information of DIBUCAINE

Product NDC: 0168-0046
Proprietary Name: DIBUCAINE
Non Proprietary Name: DIBUCAINE
Active Ingredient(s): 1    g/100g & nbsp;   DIBUCAINE
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of DIBUCAINE

Product NDC: 0168-0046
Labeler Name: E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part346
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19680101

Package Information of DIBUCAINE

Package NDC: 0168-0046-31
Package Description: 1 TUBE in 1 CARTON (0168-0046-31) > 28 g in 1 TUBE

NDC Information of DIBUCAINE

NDC Code 0168-0046-31
Proprietary Name DIBUCAINE
Package Description 1 TUBE in 1 CARTON (0168-0046-31) > 28 g in 1 TUBE
Product NDC 0168-0046
Product Type Name HUMAN OTC DRUG
Non Proprietary Name DIBUCAINE
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 19680101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
Substance Name DIBUCAINE
Strength Number 1
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of DIBUCAINE


General Information