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COLISTIMETHATE SODIUM
COLISTIMETHATE SODIUM - 23155-193-31 - (COLISTIMETHATE SODIUM)
Drug Information of COLISTIMETHATE SODIUM
| Product NDC: | 23155-193 |
| Proprietary Name: | COLISTIMETHATE SODIUM |
| Non Proprietary Name: | COLISTIMETHATE SODIUM |
| Active Ingredient(s): | 150 mg/4mL & nbsp; COLISTIMETHATE SODIUM |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of COLISTIMETHATE SODIUM
| Product NDC: | 23155-193 |
| Labeler Name: | Heritage Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202359 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121022 |
Package Information of COLISTIMETHATE SODIUM
| Package NDC: | 23155-193-31 |
| Package Description: | 1 VIAL, GLASS in 1 CARTON (23155-193-31) > 4 mL in 1 VIAL, GLASS |
NDC Information of COLISTIMETHATE SODIUM
| NDC Code | 23155-193-31 |
| Proprietary Name | COLISTIMETHATE SODIUM |
| Package Description | 1 VIAL, GLASS in 1 CARTON (23155-193-31) > 4 mL in 1 VIAL, GLASS |
| Product NDC | 23155-193 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | COLISTIMETHATE SODIUM |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20121022 |
| Marketing Category Name | ANDA |
| Labeler Name | Heritage Pharmaceuticals Inc. |
| Substance Name | COLISTIMETHATE SODIUM |
| Strength Number | 150 |
| Strength Unit | mg/4mL |
| Pharmaceutical Classes | Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient] |
