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Finafta
Finafta - 58593-781-02 - (Benzocaine)
Drug Information of Finafta
| Product NDC: | 58593-781 |
| Proprietary Name: | Finafta |
| Non Proprietary Name: | Benzocaine |
| Active Ingredient(s): | 7.5 mg/100mg & nbsp; Benzocaine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Finafta
| Product NDC: | 58593-781 |
| Labeler Name: | Efficient Laboratories Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20000101 |
Package Information of Finafta
| Package NDC: | 58593-781-02 |
| Package Description: | 7100 mg in 1 TUBE (58593-781-02) |
NDC Information of Finafta
| NDC Code | 58593-781-02 |
| Proprietary Name | Finafta |
| Package Description | 7100 mg in 1 TUBE (58593-781-02) |
| Product NDC | 58593-781 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Benzocaine |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20000101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Efficient Laboratories Inc. |
| Substance Name | BENZOCAINE |
| Strength Number | 7.5 |
| Strength Unit | mg/100mg |
| Pharmaceutical Classes |
