Product NDC: | 49349-773 |
Proprietary Name: | Ery-Tab |
Non Proprietary Name: | Erythromycin |
Active Ingredient(s): | 333 mg/1 & nbsp; Erythromycin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49349-773 |
Labeler Name: | REMEDYREPACK INC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA062298 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110819 |
Package NDC: | 49349-773-02 |
Package Description: | 30 TABLET in 1 BLISTER PACK (49349-773-02) |
NDC Code | 49349-773-02 |
Proprietary Name | Ery-Tab |
Package Description | 30 TABLET in 1 BLISTER PACK (49349-773-02) |
Product NDC | 49349-773 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Erythromycin |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20110819 |
Marketing Category Name | ANDA |
Labeler Name | REMEDYREPACK INC. |
Substance Name | ERYTHROMYCIN |
Strength Number | 333 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Macrolide [EPC],Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |