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Azithromycin
Azithromycin - 0409-0144-10 - (AZITHROMYCIN MONOHYDRATE)
Drug Information of Azithromycin
| Product NDC: | 0409-0144 |
| Proprietary Name: | Azithromycin |
| Non Proprietary Name: | AZITHROMYCIN MONOHYDRATE |
| Active Ingredient(s): | 500 mg/1 & nbsp; AZITHROMYCIN MONOHYDRATE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Azithromycin
| Product NDC: | 0409-0144 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065500 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090626 |
Package Information of Azithromycin
| Package NDC: | 0409-0144-10 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-0144-10) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE |
NDC Information of Azithromycin
| NDC Code | 0409-0144-10 |
| Proprietary Name | Azithromycin |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-0144-10) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0409-0144 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | AZITHROMYCIN MONOHYDRATE |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20090626 |
| Marketing Category Name | ANDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | AZITHROMYCIN MONOHYDRATE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |
