Product NDC: | 35356-798 |
Proprietary Name: | azithromycin |
Non Proprietary Name: | azithromycin |
Active Ingredient(s): | 500 mg/1 & nbsp; azithromycin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 35356-798 |
Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050784 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20020524 |
Package NDC: | 35356-798-03 |
Package Description: | 3 TABLET, FILM COATED in 1 BLISTER PACK (35356-798-03) |
NDC Code | 35356-798-03 |
Proprietary Name | azithromycin |
Package Description | 3 TABLET, FILM COATED in 1 BLISTER PACK (35356-798-03) |
Product NDC | 35356-798 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | azithromycin |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20020524 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
Substance Name | AZITHROMYCIN ANHYDROUS |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |