Product NDC: | 35356-017 |
Proprietary Name: | Azithromycin |
Non Proprietary Name: | Azithromycin |
Active Ingredient(s): | 500 mg/1 & nbsp; Azithromycin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35356-017 |
Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065405 |
Marketing Category: | ANDA |
Start Marketing Date: | 20101109 |
Package NDC: | 35356-017-03 |
Package Description: | 3 TABLET in 1 BLISTER PACK (35356-017-03) |
NDC Code | 35356-017-03 |
Proprietary Name | Azithromycin |
Package Description | 3 TABLET in 1 BLISTER PACK (35356-017-03) |
Product NDC | 35356-017 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Azithromycin |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20101109 |
Marketing Category Name | ANDA |
Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
Substance Name | AZITHROMYCIN |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |