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DIBUCAINE
DIBUCAINE - 59779-398-03 - (DIBUCAINE)
Drug Information of DIBUCAINE
| Product NDC: | 59779-398 |
| Proprietary Name: | DIBUCAINE |
| Non Proprietary Name: | DIBUCAINE |
| Active Ingredient(s): | 10 mg/g & nbsp; DIBUCAINE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DIBUCAINE
| Product NDC: | 59779-398 |
| Labeler Name: | CVS Pharmacy |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part346 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100716 |
Package Information of DIBUCAINE
| Package NDC: | 59779-398-03 |
| Package Description: | 1 TUBE in 1 CARTON (59779-398-03) > 28 g in 1 TUBE |
NDC Information of DIBUCAINE
| NDC Code | 59779-398-03 |
| Proprietary Name | DIBUCAINE |
| Package Description | 1 TUBE in 1 CARTON (59779-398-03) > 28 g in 1 TUBE |
| Product NDC | 59779-398 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DIBUCAINE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100716 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | CVS Pharmacy |
| Substance Name | DIBUCAINE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
