DOXYCYCLINE

Product NDC

69007-822

11-digit product format

690070822

Labeler code

69007

Product ID

69007-822_c954fd97-3e5b-4fda-8f8e-74f4fc0b1601

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

DOXYCYCLINE

Dosage form

CAPSULE

Route

ORAL

Labeler

Owen Laboratories, Inc.

Application

NDA050805

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2010-05-14

Marketing end

0000-00-00

Substance

DOXYCYCLINE

Active strength

40 mg/1

Pharmacologic classes

Tetracycline-class Drug [EPC],Tetracyclines [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record