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Doxycycline Monohydrate - 0115-1327-13 - (Doxycycline)

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Drug Information of Doxycycline Monohydrate

Product NDC: 0115-1327
Proprietary Name: Doxycycline Monohydrate
Non Proprietary Name: Doxycycline
Active Ingredient(s): 150    mg/1 & nbsp;   Doxycycline
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Doxycycline Monohydrate

Product NDC: 0115-1327
Labeler Name: Global Pharmaceuticals, Division of Impax Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200065
Marketing Category: ANDA
Start Marketing Date: 20110421

Package Information of Doxycycline Monohydrate

Package NDC: 0115-1327-13
Package Description: 60 CAPSULE in 1 BOTTLE (0115-1327-13)

NDC Information of Doxycycline Monohydrate

NDC Code 0115-1327-13
Proprietary Name Doxycycline Monohydrate
Package Description 60 CAPSULE in 1 BOTTLE (0115-1327-13)
Product NDC 0115-1327
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxycycline
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110421
Marketing Category Name ANDA
Labeler Name Global Pharmaceuticals, Division of Impax Laboratories Inc.
Substance Name DOXYCYCLINE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Doxycycline Monohydrate


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