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Mupirocin Calcium - 66993-942-31 - (mupirocin calcium)

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Drug Information of Mupirocin Calcium

Product NDC: 66993-942
Proprietary Name: Mupirocin Calcium
Non Proprietary Name: mupirocin calcium
Active Ingredient(s): 20    mg/g & nbsp;   mupirocin calcium
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Mupirocin Calcium

Product NDC: 66993-942
Labeler Name: Prasco Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050746
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20130128

Package Information of Mupirocin Calcium

Package NDC: 66993-942-31
Package Description: 1 TUBE in 1 CARTON (66993-942-31) > 30 g in 1 TUBE

NDC Information of Mupirocin Calcium

NDC Code 66993-942-31
Proprietary Name Mupirocin Calcium
Package Description 1 TUBE in 1 CARTON (66993-942-31) > 30 g in 1 TUBE
Product NDC 66993-942
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name mupirocin calcium
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20130128
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Prasco Laboratories
Substance Name MUPIROCIN CALCIUM
Strength Number 20
Strength Unit mg/g
Pharmaceutical Classes RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA]

Complete Information of Mupirocin Calcium


General Information