Mondoxyne

Product NDC

69668-432

11-digit product format

696680432

Labeler code

69668

Product ID

69668-432_6e78c15f-a68f-7038-e053-2a91aa0a98f5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Doxycycline

Dosage form

CAPSULE

Route

ORAL

Labeler

Sonoma Pharmaceuticals, Inc.

Application

ANDA204446

Marketing category

ANDA

Marketing start

2015-05-28

Marketing end

2019-09-30

Substance

DOXYCYCLINE

Active strength

75 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