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Dicloxacillin Sodium - 0093-3125-01 - (Dicloxacillin Sodium)

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Drug Information of Dicloxacillin Sodium

Product NDC: 0093-3125
Proprietary Name: Dicloxacillin Sodium
Non Proprietary Name: Dicloxacillin Sodium
Active Ingredient(s): 500    mg/1 & nbsp;   Dicloxacillin Sodium
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Dicloxacillin Sodium

Product NDC: 0093-3125
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062286
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Dicloxacillin Sodium

Package NDC: 0093-3125-01
Package Description: 100 CAPSULE in 1 BOTTLE (0093-3125-01)

NDC Information of Dicloxacillin Sodium

NDC Code 0093-3125-01
Proprietary Name Dicloxacillin Sodium
Package Description 100 CAPSULE in 1 BOTTLE (0093-3125-01)
Product NDC 0093-3125
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dicloxacillin Sodium
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name DICLOXACILLIN SODIUM
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Dicloxacillin Sodium


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