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AMPHOTEC
AMPHOTEC - 66435-301-51 - (Amphotericin B)
Drug Information of AMPHOTEC
| Product NDC: | 66435-301 |
| Proprietary Name: | AMPHOTEC |
| Non Proprietary Name: | Amphotericin B |
| Active Ingredient(s): | 50 mg/50mg & nbsp; Amphotericin B |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, LIPID COMPLEX |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AMPHOTEC
| Product NDC: | 66435-301 |
| Labeler Name: | Kadmon Pharmaceuticals LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050729 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050520 |
Package Information of AMPHOTEC
| Package NDC: | 66435-301-51 |
| Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (66435-301-51) > 50 mg in 1 VIAL, SINGLE-USE |
NDC Information of AMPHOTEC
| NDC Code | 66435-301-51 |
| Proprietary Name | AMPHOTEC |
| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (66435-301-51) > 50 mg in 1 VIAL, SINGLE-USE |
| Product NDC | 66435-301 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amphotericin B |
| Dosage Form Name | INJECTION, LIPID COMPLEX |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20050520 |
| Marketing Category Name | NDA |
| Labeler Name | Kadmon Pharmaceuticals LLC |
| Substance Name | AMPHOTERICIN B |
| Strength Number | 50 |
| Strength Unit | mg/50mg |
| Pharmaceutical Classes | Lipid-based Polyene Antifungal [EPC],Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient] |
