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Doxycycline - 0527-1335-01 - (Doxycycline)

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Drug Information of Doxycycline

Product NDC: 0527-1335
Proprietary Name: Doxycycline
Non Proprietary Name: Doxycycline
Active Ingredient(s): 50    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: 0527-1335
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065285
Marketing Category: ANDA
Start Marketing Date: 20051208

Package Information of Doxycycline

Package NDC: 0527-1335-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1335-01)

NDC Information of Doxycycline

NDC Code 0527-1335-01
Proprietary Name Doxycycline
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0527-1335-01)
Product NDC 0527-1335
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxycycline
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20051208
Marketing Category Name ANDA
Labeler Name Lannett Company, Inc.
Substance Name DOXYCYCLINE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Doxycycline


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