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Doxycycline - 21695-581-14 - (Doxycycline Hyclate)

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Drug Information of Doxycycline

Product NDC: 21695-581
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: 21695-581
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065095
Marketing Category: ANDA
Start Marketing Date: 20030702

Package Information of Doxycycline

Package NDC: 21695-581-14
Package Description: 14 TABLET, COATED in 1 BOTTLE (21695-581-14)

NDC Information of Doxycycline

NDC Code 21695-581-14
Proprietary Name Doxycycline
Package Description 14 TABLET, COATED in 1 BOTTLE (21695-581-14)
Product NDC 21695-581
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxycycline Hyclate
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20030702
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name DOXYCYCLINE HYCLATE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Doxycycline


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