Product NDC: | 0074-6316 |
Proprietary Name: | Erythrocin Stearate |
Non Proprietary Name: | Erythromycin Stearate |
Active Ingredient(s): | 500 mg/1 & nbsp; Erythromycin Stearate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0074-6316 |
Labeler Name: | Abbott Laboratories |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA060359 |
Marketing Category: | ANDA |
Start Marketing Date: | 19640624 |
Package NDC: | 0074-6316-13 |
Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (0074-6316-13) |
NDC Code | 0074-6316-13 |
Proprietary Name | Erythrocin Stearate |
Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0074-6316-13) |
Product NDC | 0074-6316 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Erythromycin Stearate |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 19640624 |
Marketing Category Name | ANDA |
Labeler Name | Abbott Laboratories |
Substance Name | ERYTHROMYCIN STEARATE |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Macrolide [EPC],Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |