Product NDC: | 59762-3051 |
Proprietary Name: | azithromycin |
Non Proprietary Name: | azithromycin |
Active Ingredient(s): | 1 g/1 & nbsp; azithromycin |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER, FOR SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59762-3051 |
Labeler Name: | Greenstone LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050693 |
Marketing Category: | NDA |
Start Marketing Date: | 19990212 |
Package NDC: | 59762-3051-2 |
Package Description: | 3 POWDER, FOR SUSPENSION in 1 BOX (59762-3051-2) |
NDC Code | 59762-3051-2 |
Proprietary Name | azithromycin |
Package Description | 3 POWDER, FOR SUSPENSION in 1 BOX (59762-3051-2) |
Product NDC | 59762-3051 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | azithromycin |
Dosage Form Name | POWDER, FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 19990212 |
Marketing Category Name | NDA |
Labeler Name | Greenstone LLC |
Substance Name | AZITHROMYCIN |
Strength Number | 1 |
Strength Unit | g/1 |
Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |