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Doxycycline Hyclate - 0172-4626-70 - (Doxycycline Hyclate)

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Drug Information of Doxycycline Hyclate

Product NDC: 0172-4626
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: 0172-4626
Labeler Name: IVAX Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065163
Marketing Category: ANDA
Start Marketing Date: 20050517

Package Information of Doxycycline Hyclate

Package NDC: 0172-4626-70
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (0172-4626-70)

NDC Information of Doxycycline Hyclate

NDC Code 0172-4626-70
Proprietary Name Doxycycline Hyclate
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (0172-4626-70)
Product NDC 0172-4626
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxycycline Hyclate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050517
Marketing Category Name ANDA
Labeler Name IVAX Pharmaceuticals, Inc.
Substance Name DOXYCYCLINE HYCLATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Doxycycline Hyclate


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