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Dicloxacillin Sodium - 52959-049-20 - (Dicloxacillin Sodium)

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Drug Information of Dicloxacillin Sodium

Product NDC: 52959-049
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: 52959-049
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062286
Marketing Category: ANDA
Start Marketing Date: 20110120

Package Information of Dicloxacillin Sodium

Package NDC: 52959-049-20
Package Description: 20 CAPSULE in 1 BOTTLE (52959-049-20)

NDC Information of Dicloxacillin Sodium

NDC Code 52959-049-20
Proprietary Name Dicloxacillin Sodium
Package Description 20 CAPSULE in 1 BOTTLE (52959-049-20)
Product NDC 52959-049
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dicloxacillin Sodium
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110120
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, 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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