Doxycycline Monohydrate

Product NDC

63629-5361

11-digit product format

636295361

Labeler code

63629

Product ID

63629-5361_ab5207ff-53ed-425b-9ef7-b8a56d411225

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Doxycycline

Dosage form

CAPSULE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

NDA050641

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2005-02-07

Marketing end

0000-00-00

Substance

DOXYCYCLINE

Active strength

100 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