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Zithromax
Zithromax - 0069-3070-75 - (AZITHROMYCIN DIHYDRATE)
Drug Information of Zithromax
| Product NDC: | 0069-3070 |
| Proprietary Name: | Zithromax |
| Non Proprietary Name: | AZITHROMYCIN DIHYDRATE |
| Active Ingredient(s): | 500 mg/1 & nbsp; AZITHROMYCIN DIHYDRATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zithromax
| Product NDC: | 0069-3070 |
| Labeler Name: | Pfizer Laboratories Div Pfizer Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050784 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20020524 |
Package Information of Zithromax
| Package NDC: | 0069-3070-75 |
| Package Description: | 3 BLISTER PACK in 1 BOX (0069-3070-75) > 3 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Zithromax
| NDC Code | 0069-3070-75 |
| Proprietary Name | Zithromax |
| Package Description | 3 BLISTER PACK in 1 BOX (0069-3070-75) > 3 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 0069-3070 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | AZITHROMYCIN DIHYDRATE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20020524 |
| Marketing Category Name | NDA |
| Labeler Name | Pfizer Laboratories Div Pfizer Inc |
| Substance Name | AZITHROMYCIN DIHYDRATE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |
