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Azithromycin
Azithromycin - 62756-512-44 - (Azithromycin)
Drug Information of Azithromycin
| Product NDC: | 62756-512 |
| Proprietary Name: | Azithromycin |
| Non Proprietary Name: | Azithromycin |
| Active Ingredient(s): | 500 mg/5mL & nbsp; Azithromycin |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Azithromycin
| Product NDC: | 62756-512 |
| Labeler Name: | Sun Pharmaceutical Industries Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090923 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130403 |
Package Information of Azithromycin
| Package NDC: | 62756-512-44 |
| Package Description: | 10 VIAL in 1 PACKAGE (62756-512-44) > 5 mL in 1 VIAL (62756-512-40) |
NDC Information of Azithromycin
| NDC Code | 62756-512-44 |
| Proprietary Name | Azithromycin |
| Package Description | 10 VIAL in 1 PACKAGE (62756-512-44) > 5 mL in 1 VIAL (62756-512-40) |
| Product NDC | 62756-512 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Azithromycin |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20130403 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharmaceutical Industries Limited |
| Substance Name | AZITHROMYCIN MONOHYDRATE |
| Strength Number | 500 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |
