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Doxycycline Hyclate - 0527-1336-10 - (Doxycycline Hyclate)

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Drug Information of Doxycycline Hyclate

Product NDC: 0527-1336
Proprietary Name: Doxycycline Hyclate
Non Proprietary Name: Doxycycline Hyclate
Active Ingredient(s): 20    mg/1 & nbsp;   Doxycycline Hyclate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Doxycycline Hyclate

Product NDC: 0527-1336
Labeler Name: Lannett Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065277
Marketing Category: ANDA
Start Marketing Date: 20051110

Package Information of Doxycycline Hyclate

Package NDC: 0527-1336-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (0527-1336-10)

NDC Information of Doxycycline Hyclate

NDC Code 0527-1336-10
Proprietary Name Doxycycline Hyclate
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (0527-1336-10)
Product NDC 0527-1336
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxycycline Hyclate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20051110
Marketing Category Name ANDA
Labeler Name Lannett Company, Inc.
Substance Name DOXYCYCLINE HYCLATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Doxycycline Hyclate


General Information