Product NDC: | 54868-0018 |
Proprietary Name: | Erythromycin Ethylsuccinate |
Non Proprietary Name: | erythromycin ethylsuccinate |
Active Ingredient(s): | 400 mg/1 & nbsp; erythromycin ethylsuccinate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-0018 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA061904 |
Marketing Category: | ANDA |
Start Marketing Date: | 19960227 |
Package NDC: | 54868-0018-3 |
Package Description: | 20 TABLET in 1 BOTTLE (54868-0018-3) |
NDC Code | 54868-0018-3 |
Proprietary Name | Erythromycin Ethylsuccinate |
Package Description | 20 TABLET in 1 BOTTLE (54868-0018-3) |
Product NDC | 54868-0018 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | erythromycin ethylsuccinate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19960227 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | ERYTHROMYCIN ETHYLSUCCINATE |
Strength Number | 400 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Macrolide [EPC],Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |