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Zithromax
Zithromax - 0069-3150-14 - (azithromycin dihydrate)
Drug Information of Zithromax
| Product NDC: | 0069-3150 |
| Proprietary Name: | Zithromax |
| Non Proprietary Name: | azithromycin dihydrate |
| Active Ingredient(s): | 500 mg/5mL & nbsp; azithromycin dihydrate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zithromax
| Product NDC: | 0069-3150 |
| Labeler Name: | Pfizer Laboratories Div Pfizer Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050733 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19970130 |
Package Information of Zithromax
| Package NDC: | 0069-3150-14 |
| Package Description: | 10 VIAL in 1 CARTON (0069-3150-14) > 5 mL in 1 VIAL |
NDC Information of Zithromax
| NDC Code | 0069-3150-14 |
| Proprietary Name | Zithromax |
| Package Description | 10 VIAL in 1 CARTON (0069-3150-14) > 5 mL in 1 VIAL |
| Product NDC | 0069-3150 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | azithromycin dihydrate |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19970130 |
| Marketing Category Name | NDA |
| Labeler Name | Pfizer Laboratories Div Pfizer Inc |
| Substance Name | AZITHROMYCIN DIHYDRATE |
| Strength Number | 500 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |
