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