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NDC 70934-0808-20 Doxycycline 100 mg/1 Details

Doxycycline 100 mg/1

Doxycycline is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is DOXYCYCLINE.

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: 70934-0808-20
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Doxycycline

Product Information

NDC	70934-0808
Product ID	70934-808_f1868678-9c16-3c52-e053-2995a90a5825
Associated GPIs	04000020000310
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
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	100
Active Ingredient Units	mg/1
Substance Name	DOXYCYCLINE
Labeler Name	Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Pharmaceutical Class	Tetracycline-class Drug [EPC], Tetracyclines [CS]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA065285
Listing Certified Through	n/a

Package

NDC 70934-0808-20 (70934080820)

Pricing Information	N/A
NDC Package Code	70934-808-20
Billing NDC	70934080820
Package	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-808-20)
Marketing Start Date	2020-12-04
NDC Exclude Flag	N