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Doxycycline - 0378-6023-89 - (Doxycycline)

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Drug Information of Doxycycline

Product NDC: 0378-6023
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: 0378-6023
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065377
Marketing Category: ANDA
Start Marketing Date: 20110504

Package Information of Doxycycline

Package NDC: 0378-6023-89
Package Description: 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6023-89)

NDC Information of Doxycycline

NDC Code 0378-6023-89
Proprietary Name Doxycycline
Package Description 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6023-89)
Product NDC 0378-6023
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxycycline
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110504
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name DOXYCYCLINE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Doxycycline


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