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AMOXICILLIN AND CLAVULANATE POTASSIUM - 68788-9847-7 - (amoxicillin and clavulanate potassium)

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Drug Information of AMOXICILLIN AND CLAVULANATE POTASSIUM

Product NDC: 68788-9847
Proprietary Name: AMOXICILLIN AND CLAVULANATE POTASSIUM
Non Proprietary Name: amoxicillin and clavulanate potassium
Active Ingredient(s): 600; 42.9    mg/5mL; mg/5mL & nbsp;   amoxicillin and clavulanate potassium
Administration Route(s): ORAL
Dosage Form(s): POWDER
Coding System: National Drug Codes(NDC)

Labeler Information of AMOXICILLIN AND CLAVULANATE POTASSIUM

Product NDC: 68788-9847
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050755
Marketing Category: NDA
Start Marketing Date: 20120330

Package Information of AMOXICILLIN AND CLAVULANATE POTASSIUM

Package NDC: 68788-9847-7
Package Description: 75 mL in 1 BOTTLE (68788-9847-7)

NDC Information of AMOXICILLIN AND CLAVULANATE POTASSIUM

NDC Code 68788-9847-7
Proprietary Name AMOXICILLIN AND CLAVULANATE POTASSIUM
Package Description 75 mL in 1 BOTTLE (68788-9847-7)
Product NDC 68788-9847
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amoxicillin and clavulanate potassium
Dosage Form Name POWDER
Route Name ORAL
Start Marketing Date 20120330
Marketing Category Name NDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name AMOXICILLIN; CLAVULANATE POTASSIUM
Strength Number 600; 42.9
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA]

Complete Information of AMOXICILLIN AND CLAVULANATE POTASSIUM


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