Home
>
National Drug Code (NDC)
>
ANBESOL MAXIMUM STRENGTH LIQUID
ANBESOL MAXIMUM STRENGTH LIQUID - 0573-0215-41 - (benzocaine)
Drug Information of ANBESOL MAXIMUM STRENGTH LIQUID
| Product NDC: | 0573-0215 |
| Proprietary Name: | ANBESOL MAXIMUM STRENGTH LIQUID |
| Non Proprietary Name: | benzocaine |
| Active Ingredient(s): | 200 mg/mL & nbsp; benzocaine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ANBESOL MAXIMUM STRENGTH LIQUID
| Product NDC: | 0573-0215 |
| Labeler Name: | Wyeth Consumer Healthcare |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20050511 |
Package Information of ANBESOL MAXIMUM STRENGTH LIQUID
| Package NDC: | 0573-0215-41 |
| Package Description: | 1 BOTTLE in 1 BLISTER PACK (0573-0215-41) > 12 mL in 1 BOTTLE |
NDC Information of ANBESOL MAXIMUM STRENGTH LIQUID
| NDC Code | 0573-0215-41 |
| Proprietary Name | ANBESOL MAXIMUM STRENGTH LIQUID |
| Package Description | 1 BOTTLE in 1 BLISTER PACK (0573-0215-41) > 12 mL in 1 BOTTLE |
| Product NDC | 0573-0215 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | benzocaine |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20050511 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Wyeth Consumer Healthcare |
| Substance Name | BENZOCAINE |
| Strength Number | 200 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
