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Doxycycline - 49884-727-04 - (doxycycline)

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Drug Information of Doxycycline

Product NDC: 49884-727
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: 49884-727
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065055
Marketing Category: ANDA
Start Marketing Date: 20001201

Package Information of Doxycycline

Package NDC: 49884-727-04
Package Description: 250 CAPSULE in 1 BOTTLE (49884-727-04)

NDC Information of Doxycycline

NDC Code 49884-727-04
Proprietary Name Doxycycline
Package Description 250 CAPSULE in 1 BOTTLE (49884-727-04)
Product NDC 49884-727
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name doxycycline
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20001201
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical Inc.
Substance Name DOXYCYCLINE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Doxycycline


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