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Doxycycline - 49999-020-20 - (Doxycycline hyclate)

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Drug Information of Doxycycline

Product NDC: 49999-020
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: 49999-020
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065095
Marketing Category: ANDA
Start Marketing Date: 20111207

Package Information of Doxycycline

Package NDC: 49999-020-20
Package Description: 20 TABLET, COATED in 1 BOTTLE (49999-020-20)

NDC Information of Doxycycline

NDC Code 49999-020-20
Proprietary Name Doxycycline
Package Description 20 TABLET, COATED in 1 BOTTLE (49999-020-20)
Product NDC 49999-020
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxycycline hyclate
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20111207
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name DOXYCYCLINE HYCLATE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Doxycycline


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