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DOXYCYCLINE - 23155-134-05 - (DOXYCYCLINE)

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Drug Information of DOXYCYCLINE

Product NDC: 23155-134
Proprietary Name: DOXYCYCLINE
Non Proprietary Name: DOXYCYCLINE
Active Ingredient(s): 75    mg/1 & nbsp;   DOXYCYCLINE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of DOXYCYCLINE

Product NDC: 23155-134
Labeler Name: Heritage Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091605
Marketing Category: ANDA
Start Marketing Date: 20120105

Package Information of DOXYCYCLINE

Package NDC: 23155-134-05
Package Description: 500 TABLET in 1 BOTTLE (23155-134-05)

NDC Information of DOXYCYCLINE

NDC Code 23155-134-05
Proprietary Name DOXYCYCLINE
Package Description 500 TABLET in 1 BOTTLE (23155-134-05)
Product NDC 23155-134
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DOXYCYCLINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120105
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals Inc.
Substance Name DOXYCYCLINE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of DOXYCYCLINE


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