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Azithromycin
Azithromycin - 60505-6076-4 - (azithromycin for injection injection, powder, lyophilized, for solution)
Drug Information of Azithromycin
| Product NDC: | 60505-6076 |
| Proprietary Name: | Azithromycin |
| Non Proprietary Name: | azithromycin for injection injection, powder, lyophilized, for solution |
| Active Ingredient(s): | 500 mg/10mL & nbsp; azithromycin for injection injection, powder, lyophilized, for solution |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Azithromycin
| Product NDC: | 60505-6076 |
| Labeler Name: | APOTEX CORP. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065501 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100425 |
Package Information of Azithromycin
| Package NDC: | 60505-6076-4 |
| Package Description: | 10 VIAL in 1 CARTON (60505-6076-4) > 10 mL in 1 VIAL |
NDC Information of Azithromycin
| NDC Code | 60505-6076-4 |
| Proprietary Name | Azithromycin |
| Package Description | 10 VIAL in 1 CARTON (60505-6076-4) > 10 mL in 1 VIAL |
| Product NDC | 60505-6076 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | azithromycin for injection injection, powder, lyophilized, for solution |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100425 |
| Marketing Category Name | ANDA |
| Labeler Name | APOTEX CORP. |
| Substance Name | AZITHROMYCIN MONOHYDRATE |
| Strength Number | 500 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |
