Home > National Drug Code (NDC) > Doxycycline

Doxycycline - 63304-130-10 - (Doxycycline)

Alphabetical Index


Drug Information of Doxycycline

Product NDC: 63304-130
Proprietary Name: Doxycycline
Non Proprietary Name: Doxycycline
Active Ingredient(s): 50    mg/1 & nbsp;   Doxycycline
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Doxycycline

Product NDC: 63304-130
Labeler Name: Ranbaxy Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065356
Marketing Category: ANDA
Start Marketing Date: 20061005

Package Information of Doxycycline

Package NDC: 63304-130-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (63304-130-10)

NDC Information of Doxycycline

NDC Code 63304-130-10
Proprietary Name Doxycycline
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (63304-130-10)
Product NDC 63304-130
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxycycline
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20061005
Marketing Category Name ANDA
Labeler Name Ranbaxy Pharmaceuticals Inc.
Substance Name DOXYCYCLINE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Doxycycline


General Information