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Doxycycline Hyclate - 23155-141-06 - (Doxycycline Hyclate)

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Drug Information of Doxycycline Hyclate

Product NDC: 23155-141
Proprietary Name: Doxycycline Hyclate
Non Proprietary Name: Doxycycline Hyclate
Active Ingredient(s): 75    mg/1 & nbsp;   Doxycycline Hyclate
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Doxycycline Hyclate

Product NDC: 23155-141
Labeler Name: Heritage Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200856
Marketing Category: ANDA
Start Marketing Date: 20130430

Package Information of Doxycycline Hyclate

Package NDC: 23155-141-06
Package Description: 60 TABLET, DELAYED RELEASE in 1 BOTTLE (23155-141-06)

NDC Information of Doxycycline Hyclate

NDC Code 23155-141-06
Proprietary Name Doxycycline Hyclate
Package Description 60 TABLET, DELAYED RELEASE in 1 BOTTLE (23155-141-06)
Product NDC 23155-141
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxycycline Hyclate
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20130430
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals Inc.
Substance Name DOXYCYCLINE HYCLATE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Doxycycline Hyclate


General Information