Doxycycline

Product NDC

49884-236

11-digit product format

498840236

Labeler code

49884

Product ID

49884-236_465e3d6a-878a-41e4-b23f-4726afbb4399

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

doxycycline

Dosage form

TABLET

Route

ORAL

Labeler

Par Pharmaceutical, Inc.

Application

ANDA065070

Marketing category

ANDA

Marketing start

2000-12-15

Marketing end

2020-06-30

Substance

DOXYCYCLINE

Active strength

150 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record