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Azithromycin Dihydrate
Azithromycin Dihydrate - 60505-2582-2 - (azithromycin)
Drug Information of Azithromycin Dihydrate
| Product NDC: | 60505-2582 |
| Proprietary Name: | Azithromycin Dihydrate |
| Non Proprietary Name: | azithromycin |
| Active Ingredient(s): | 500 mg/1 & nbsp; azithromycin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Azithromycin Dihydrate
| Product NDC: | 60505-2582 |
| Labeler Name: | Apotex Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065509 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110718 |
Package Information of Azithromycin Dihydrate
| Package NDC: | 60505-2582-2 |
| Package Description: | 3 BLISTER PACK in 1 PACKAGE (60505-2582-2) > 3 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Azithromycin Dihydrate
| NDC Code | 60505-2582-2 |
| Proprietary Name | Azithromycin Dihydrate |
| Package Description | 3 BLISTER PACK in 1 PACKAGE (60505-2582-2) > 3 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 60505-2582 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | azithromycin |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110718 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotex Corp. |
| Substance Name | AZITHROMYCIN DIHYDRATE |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |
