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Chloramphenicol Sodium Succinate
Chloramphenicol Sodium Succinate - 63323-011-15 - (CHLORAMPHENICOL SODIUM SUCCINATE)
Drug Information of Chloramphenicol Sodium Succinate
| Product NDC: | 63323-011 |
| Proprietary Name: | Chloramphenicol Sodium Succinate |
| Non Proprietary Name: | CHLORAMPHENICOL SODIUM SUCCINATE |
| Active Ingredient(s): | 1 g/10mL & nbsp; CHLORAMPHENICOL SODIUM SUCCINATE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Chloramphenicol Sodium Succinate
| Product NDC: | 63323-011 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062365 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010112 |
Package Information of Chloramphenicol Sodium Succinate
| Package NDC: | 63323-011-15 |
| Package Description: | 10 VIAL in 1 TRAY (63323-011-15) > 10 mL in 1 VIAL |
NDC Information of Chloramphenicol Sodium Succinate
| NDC Code | 63323-011-15 |
| Proprietary Name | Chloramphenicol Sodium Succinate |
| Package Description | 10 VIAL in 1 TRAY (63323-011-15) > 10 mL in 1 VIAL |
| Product NDC | 63323-011 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CHLORAMPHENICOL SODIUM SUCCINATE |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20010112 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | CHLORAMPHENICOL SODIUM SUCCINATE |
| Strength Number | 1 |
| Strength Unit | g/10mL |
| Pharmaceutical Classes | Amphenicol-class Antibacterial [EPC],Amphenicols [Chemical/Ingredient] |
