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Doxycycline - 52125-433-02 - (doxycycline)

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Drug Information of Doxycycline

Product NDC: 52125-433
Proprietary Name: Doxycycline
Non Proprietary Name: doxycycline
Active Ingredient(s): 100    mg/1 & nbsp;   doxycycline
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Doxycycline

Product NDC: 52125-433
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065055
Marketing Category: ANDA
Start Marketing Date: 20130515

Package Information of Doxycycline

Package NDC: 52125-433-02
Package Description: 30 CAPSULE in 1 BLISTER PACK (52125-433-02)

NDC Information of Doxycycline

NDC Code 52125-433-02
Proprietary Name Doxycycline
Package Description 30 CAPSULE in 1 BLISTER PACK (52125-433-02)
Product NDC 52125-433
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name doxycycline
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130515
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name DOXYCYCLINE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Doxycycline


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