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Doxycycline - 24658-220-20 - (Doxycycline hyclate)

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Drug Information of Doxycycline

Product NDC: 24658-220
Proprietary Name: Doxycycline
Non Proprietary Name: Doxycycline hyclate
Active Ingredient(s): 100    mg/1 & nbsp;   Doxycycline hyclate
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Doxycycline

Product NDC: 24658-220
Labeler Name: Blu Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065095
Marketing Category: ANDA
Start Marketing Date: 20100501

Package Information of Doxycycline

Package NDC: 24658-220-20
Package Description: 20 TABLET, COATED in 1 BOTTLE (24658-220-20)

NDC Information of Doxycycline

NDC Code 24658-220-20
Proprietary Name Doxycycline
Package Description 20 TABLET, COATED in 1 BOTTLE (24658-220-20)
Product NDC 24658-220
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxycycline hyclate
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20100501
Marketing Category Name ANDA
Labeler Name Blu Pharmaceuticals, LLC
Substance Name DOXYCYCLINE HYCLATE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Doxycycline


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