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Doxycycline Hyclate - 68645-020-20 - (Doxycycline Hyclate)

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Drug Information of Doxycycline Hyclate

Product NDC: 68645-020
Proprietary Name: Doxycycline Hyclate
Non Proprietary Name: Doxycycline Hyclate
Active Ingredient(s): 100    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: 68645-020
Labeler Name: Legacy Pharmaceutical Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062505
Marketing Category: ANDA
Start Marketing Date: 20110209

Package Information of Doxycycline Hyclate

Package NDC: 68645-020-20
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (68645-020-20)

NDC Information of Doxycycline Hyclate

NDC Code 68645-020-20
Proprietary Name Doxycycline Hyclate
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (68645-020-20)
Product NDC 68645-020
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxycycline Hyclate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110209
Marketing Category Name ANDA
Labeler Name Legacy Pharmaceutical Packaging
Substance Name DOXYCYCLINE HYCLATE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Doxycycline Hyclate


General Information