AMPHOTEC - 66435-302-01 - (Amphotericin B)

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Drug Information of AMPHOTEC

Product NDC: 66435-302
Proprietary Name: AMPHOTEC
Non Proprietary Name: Amphotericin B
Active Ingredient(s): 100    mg/100mg & 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: 66435-302
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: 66435-302-01
Package Description: 1 VIAL, SINGLE-USE in 1 CARTON (66435-302-01) > 100 mg in 1 VIAL, SINGLE-USE

NDC Information of AMPHOTEC

NDC Code 66435-302-01
Proprietary Name AMPHOTEC
Package Description 1 VIAL, SINGLE-USE in 1 CARTON (66435-302-01) > 100 mg in 1 VIAL, SINGLE-USE
Product NDC 66435-302
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 100
Strength Unit mg/100mg
Pharmaceutical Classes Lipid-based Polyene Antifungal [EPC],Polyene Antifungal [EPC],Polyenes [Chemical/Ingredient]

Complete Information of AMPHOTEC


General Information