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Doxycycline - 49884-092-05 - (doxycycline)

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Drug Information of Doxycycline

Product NDC: 49884-092
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: 49884-092
Labeler Name: Par Pharmaceutical Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065070
Marketing Category: ANDA
Start Marketing Date: 20001215

Package Information of Doxycycline

Package NDC: 49884-092-05
Package Description: 500 TABLET in 1 BOTTLE (49884-092-05)

NDC Information of Doxycycline

NDC Code 49884-092-05
Proprietary Name Doxycycline
Package Description 500 TABLET in 1 BOTTLE (49884-092-05)
Product NDC 49884-092
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name doxycycline
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20001215
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical Inc
Substance Name DOXYCYCLINE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Doxycycline


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