Product NDC: | 35356-704 |
Proprietary Name: | Azithromycin |
Non Proprietary Name: | Azithromycin |
Active Ingredient(s): | 250 mg/1 & nbsp; Azithromycin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35356-704 |
Labeler Name: | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065211 |
Marketing Category: | ANDA |
Start Marketing Date: | 20051114 |
Package NDC: | 35356-704-06 |
Package Description: | 6 TABLET, FILM COATED in 1 BLISTER PACK (35356-704-06) |
NDC Code | 35356-704-06 |
Proprietary Name | Azithromycin |
Package Description | 6 TABLET, FILM COATED in 1 BLISTER PACK (35356-704-06) |
Product NDC | 35356-704 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Azithromycin |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20051114 |
Marketing Category Name | ANDA |
Labeler Name | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | AZITHROMYCIN MONOHYDRATE |
Strength Number | 250 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |