Monodox - 16110-075-01 - (doxycycline)

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Drug Information of Monodox

Product NDC: 16110-075
Proprietary Name: Monodox
Non Proprietary Name: doxycycline
Active Ingredient(s): 75    mg/1 & nbsp;   doxycycline
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Monodox

Product NDC: 16110-075
Labeler Name: Aqua Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050641
Marketing Category: NDA
Start Marketing Date: 20070131

Package Information of Monodox

Package NDC: 16110-075-01
Package Description: 100 CAPSULE in 1 BOTTLE (16110-075-01)

NDC Information of Monodox

NDC Code 16110-075-01
Proprietary Name Monodox
Package Description 100 CAPSULE in 1 BOTTLE (16110-075-01)
Product NDC 16110-075
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name doxycycline
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20070131
Marketing Category Name NDA
Labeler Name Aqua Pharmaceuticals, LLC
Substance Name DOXYCYCLINE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Monodox


General Information