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Erythrocin Stearate
Erythrocin Stearate - 24338-106-20 - (ERYTHROMYCIN STEARATE)
Drug Information of Erythrocin Stearate
| Product NDC: | 24338-106 |
| Proprietary Name: | Erythrocin Stearate |
| Non Proprietary Name: | ERYTHROMYCIN STEARATE |
| Active Ingredient(s): | 250 mg/1 & nbsp; ERYTHROMYCIN STEARATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Erythrocin Stearate
| Product NDC: | 24338-106 |
| Labeler Name: | Arbor Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA060359 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110801 |
Package Information of Erythrocin Stearate
| Package NDC: | 24338-106-20 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (24338-106-20) |
NDC Information of Erythrocin Stearate
| NDC Code | 24338-106-20 |
| Proprietary Name | Erythrocin Stearate |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (24338-106-20) |
| Product NDC | 24338-106 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ERYTHROMYCIN STEARATE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110801 |
| Marketing Category Name | ANDA |
| Labeler Name | Arbor Pharmaceuticals, Inc. |
| Substance Name | ERYTHROMYCIN STEARATE |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Macrolide [EPC],Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |
