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ERYTHROMYCIN
ERYTHROMYCIN - 16590-091-90 - (ERYTHROMYCIN)
Drug Information of ERYTHROMYCIN
| Product NDC: | 16590-091 |
| Proprietary Name: | ERYTHROMYCIN |
| Non Proprietary Name: | ERYTHROMYCIN |
| Active Ingredient(s): | 250 mg/1 & nbsp; ERYTHROMYCIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ERYTHROMYCIN
| Product NDC: | 16590-091 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA061621 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19720711 |
Package Information of ERYTHROMYCIN
| Package NDC: | 16590-091-90 |
| Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE (16590-091-90) |
NDC Information of ERYTHROMYCIN
| NDC Code | 16590-091-90 |
| Proprietary Name | ERYTHROMYCIN |
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (16590-091-90) |
| Product NDC | 16590-091 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ERYTHROMYCIN |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19720711 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | ERYTHROMYCIN |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Macrolide [EPC],Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |
