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NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE - 48102-003-35 - (NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE)

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Drug Information of NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE

Product NDC: 48102-003
Proprietary Name: NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE
Non Proprietary Name: NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE
Active Ingredient(s): 1; 3.5; 10000    mg/g; mg/g; U/g & nbsp;   NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE
Administration Route(s): OPHTHALMIC
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE

Product NDC: 48102-003
Labeler Name: Fera Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062938
Marketing Category: ANDA
Start Marketing Date: 20110720

Package Information of NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE

Package NDC: 48102-003-35
Package Description: 1 TUBE in 1 CARTON (48102-003-35) > 3.5 g in 1 TUBE

NDC Information of NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE

NDC Code 48102-003-35
Proprietary Name NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE
Package Description 1 TUBE in 1 CARTON (48102-003-35) > 3.5 g in 1 TUBE
Product NDC 48102-003
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NEOMYCIN AND POLYMYXIN B SULFATES AND DEXAMETHASONE
Dosage Form Name OINTMENT
Route Name OPHTHALMIC
Start Marketing Date 20110720
Marketing Category Name ANDA
Labeler Name Fera Pharmaceuticals
Substance Name DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Strength Number 1; 3.5; 10000
Strength Unit mg/g; mg/g; U/g
Pharmaceutical Classes Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

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