Home
>
National Drug Code (NDC)
>
Amphotericin B
Amphotericin B - 39822-1055-5 - (Amphotericin B)
Drug Information of Amphotericin B
| Product NDC: | 39822-1055 |
| Proprietary Name: | Amphotericin B |
| Non Proprietary Name: | Amphotericin B |
| Active Ingredient(s): | 50 mg/10mL & nbsp; Amphotericin B |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amphotericin B
| Product NDC: | 39822-1055 |
| Labeler Name: | X-GEN Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA063206 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19920429 |
Package Information of Amphotericin B
| Package NDC: | 39822-1055-5 |
| Package Description: | 10 mL in 1 VIAL (39822-1055-5) |
NDC Information of Amphotericin B
| NDC Code | 39822-1055-5 |
| Proprietary Name | Amphotericin B |
| Package Description | 10 mL in 1 VIAL (39822-1055-5) |
| Product NDC | 39822-1055 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amphotericin B |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19920429 |
| Marketing Category Name | ANDA |
| Labeler Name | X-GEN Pharmaceuticals, Inc. |
| Substance Name | AMPHOTERICIN B |
| Strength Number | 50 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes | Lipid-based Polyene Antifungal [EPC],Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient] |
