Doxycycline Monohydrate

Product NDC

43063-789

11-digit product format

430630789

Labeler code

43063

Product ID

43063-789_959532f3-e3aa-2cea-e053-2a95a90ad132

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Doxycycline

Dosage form

CAPSULE

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

NDA050641

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2005-02-07

Marketing end

0000-00-00

Substance

DOXYCYCLINE

Active strength

50 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record