Product NDC: | 52125-538 |
Proprietary Name: | Erythromycin |
Non Proprietary Name: | Erythromycin |
Active Ingredient(s): | 5 mg/g & nbsp; Erythromycin |
Administration Route(s): | OPHTHALMIC |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52125-538 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA064067 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130506 |
Package NDC: | 52125-538-01 |
Package Description: | 3.5 g in 1 CARTON (52125-538-01) |
NDC Code | 52125-538-01 |
Proprietary Name | Erythromycin |
Package Description | 3.5 g in 1 CARTON (52125-538-01) |
Product NDC | 52125-538 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Erythromycin |
Dosage Form Name | OINTMENT |
Route Name | OPHTHALMIC |
Start Marketing Date | 20130506 |
Marketing Category Name | ANDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | ERYTHROMYCIN |
Strength Number | 5 |
Strength Unit | mg/g |
Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Macrolide [EPC],Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |