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ZITHROMAX
ZITHROMAX - 0069-3051-07 - (AZITHROMYCIN DIHYDRATE)
Drug Information of ZITHROMAX
| Product NDC: | 0069-3051 |
| Proprietary Name: | ZITHROMAX |
| Non Proprietary Name: | AZITHROMYCIN DIHYDRATE |
| Active Ingredient(s): | 1 g/1 & nbsp; AZITHROMYCIN DIHYDRATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZITHROMAX
| Product NDC: | 0069-3051 |
| Labeler Name: | Pfizer Laboratories Div Pfizer Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050693 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19940928 |
Package Information of ZITHROMAX
| Package NDC: | 0069-3051-07 |
| Package Description: | 10 PACKET in 1 BOX (0069-3051-07) > 1 POWDER, FOR SUSPENSION in 1 PACKET |
NDC Information of ZITHROMAX
| NDC Code | 0069-3051-07 |
| Proprietary Name | ZITHROMAX |
| Package Description | 10 PACKET in 1 BOX (0069-3051-07) > 1 POWDER, FOR SUSPENSION in 1 PACKET |
| Product NDC | 0069-3051 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | AZITHROMYCIN DIHYDRATE |
| Dosage Form Name | POWDER, FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 19940928 |
| Marketing Category Name | NDA |
| Labeler Name | Pfizer Laboratories Div Pfizer Inc |
| Substance Name | AZITHROMYCIN DIHYDRATE |
| Strength Number | 1 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |
