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Doxycycline Hyclate - 53489-647-07 - (Doxycycline Hyclate)

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Drug Information of Doxycycline Hyclate

Product NDC: 53489-647
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: 53489-647
Labeler Name: Mutual Pharmaceutical Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065134
Marketing Category: ANDA
Start Marketing Date: 20050513

Package Information of Doxycycline Hyclate

Package NDC: 53489-647-07
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-07)

NDC Information of Doxycycline Hyclate

NDC Code 53489-647-07
Proprietary Name Doxycycline Hyclate
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-647-07)
Product NDC 53489-647
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxycycline Hyclate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050513
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical Company, Inc.
Substance Name DOXYCYCLINE HYCLATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Doxycycline Hyclate


General Information