Search by Drug Name or NDC

NDC 51655-0998-20 Doxycycline 100 mg/1 Details

Doxycycline 100 mg/1

Doxycycline is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals, LLC. The primary component is DOXYCYCLINE HYCLATE.

MedlinePlus Drug Summary

Doxycycline is used to treat a variety of infections caused by certain types of bacteria. Doxycycline is also used to treat or prevent anthrax (a serious infection that may be spread on purpose as part of a bioterror attack) in people who may have been exposed to anthrax in the air and to treat plague and tuleramia (serious infections that may be spread on purpose as part of a bioterror attack). It is also used to prevent malaria. Doxycycline is also used along with other medications to treat acne and rosacea (a skin disease that causes redness, flushing, and pimples on the face). Doxycycline (Oracea) is used only to treat pimples and bumps caused by rosacea. Doxycycline is in a class of medications called tetracycline antibiotics. It works to treat infections by preventing the growth and spread of bacteria. It works to treat acne by killing the bacteria that infects pores and decreasing a certain natural oily substance that causes acne. It works to treat rosacea by decreasing the inflammation that causes this condition. Antibiotics such as doxycycline will not work for colds, flu, or other viral infections. Using antibiotics when they are not needed increases your risk of getting an infection later that resists antibiotic treatment.

Related Packages: 51655-0998-20
Last Updated: 04/21/2024
MedLinePlus Full Drug Details: Doxycycline

Product Information

NDC	51655-0998
Product ID	51655-998_fe070e2e-3e75-fb84-e053-6294a90afd88
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Doxycycline
Proprietary Name Suffix	n/a
Non-Proprietary Name	Doxycycline hyclate
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, COATED
Route	ORAL
Active Ingredient Strength	100
Active Ingredient Units	mg/1
Substance Name	DOXYCYCLINE HYCLATE
Labeler Name	Northwind Pharmaceuticals, LLC
Pharmaceutical Class	Tetracycline-class Drug [EPC], Tetracyclines [CS]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA065095
Listing Certified Through	2024-12-31

Package

NDC 51655-0998-20 (51655099820)

Pricing Information	N/A
NDC Package Code	51655-998-20
Billing NDC	51655099820
Package	20 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-998-20)
Marketing Start Date	2023-06-08
NDC Exclude Flag	N