Doxycycline

Product NDC

53002-0670

11-digit product format

530020670

Labeler code

53002

Product ID

53002-0670_64f70a1a-d1e0-40b3-ac94-737cbb9affbb

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Doxycycline

Dosage form

CAPSULE

Route

ORAL

Labeler

RPK Pharmaceuticals, Inc.

Application

ANDA204446

Marketing category

ANDA

Marketing start

2016-04-29

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

2021-12-31

Current FDA listing

Historical FDA.report record