Doxycycline

Product NDC

67405-475

11-digit product format

674050475

Labeler code

67405

Product ID

67405-475_02f1de9a-fd4c-48d2-b60a-cf11629b316a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

DOXYCYCLINE

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

Harris Pharmaceutical, Inc

Application

ANDA065454

Marketing category

ANDA

Marketing start

2008-07-16

Marketing end

0000-00-00

Substance

DOXYCYCLINE

Active strength

25 mg/5mL

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