| Product NDC: | 68258-3051 | 
| 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: | 68258-3051 | 
| Labeler Name: | Dispensing Solutions, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | NDA050693 | 
| Marketing Category: | NDA | 
| Start Marketing Date: | 19990212 | 
| Package NDC: | 68258-3051-1 | 
| Package Description: | 10 POWDER, FOR SUSPENSION in 1 BOX (68258-3051-1) | 
| NDC Code | 68258-3051-1 | 
| Proprietary Name | azithromycin | 
| Package Description | 10 POWDER, FOR SUSPENSION in 1 BOX (68258-3051-1) | 
| Product NDC | 68258-3051 | 
| 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 | Dispensing Solutions, Inc. | 
| Substance Name | AZITHROMYCIN | 
| Strength Number | 1 | 
| Strength Unit | g/1 | 
| Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |