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Dicloxacillin Sodium - 0781-2248-01 - (Dicloxacillin Sodium)

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Drug Information of Dicloxacillin Sodium

Product NDC: 0781-2248
Proprietary Name: Dicloxacillin Sodium
Non Proprietary Name: Dicloxacillin Sodium
Active Ingredient(s): 250    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: 0781-2248
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA061454
Marketing Category: ANDA
Start Marketing Date: 19710401

Package Information of Dicloxacillin Sodium

Package NDC: 0781-2248-01
Package Description: 100 CAPSULE in 1 BOTTLE (0781-2248-01)

NDC Information of Dicloxacillin Sodium

NDC Code 0781-2248-01
Proprietary Name Dicloxacillin Sodium
Package Description 100 CAPSULE in 1 BOTTLE (0781-2248-01)
Product NDC 0781-2248
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dicloxacillin Sodium
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19710401
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name DICLOXACILLIN SODIUM
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Dicloxacillin Sodium


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