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Doxycycline - 0179-0129-20 - (Doxycycline)

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Drug Information of Doxycycline

Product NDC: 0179-0129
Proprietary Name: Doxycycline
Non Proprietary Name: Doxycycline
Active Ingredient(s): 100    mg/1 & nbsp;   Doxycycline
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Doxycycline

Product NDC: 0179-0129
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065285
Marketing Category: ANDA
Start Marketing Date: 20130314

Package Information of Doxycycline

Package NDC: 0179-0129-20
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (0179-0129-20)

NDC Information of Doxycycline

NDC Code 0179-0129-20
Proprietary Name Doxycycline
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (0179-0129-20)
Product NDC 0179-0129
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxycycline
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130314
Marketing Category Name ANDA
Labeler Name KAISER FOUNDATION HOSPITALS
Substance Name DOXYCYCLINE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Doxycycline


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