Doxycycline

Product NDC

70518-0221

11-digit product format

705180221

Labeler code

70518

Product ID

70518-0221_9fda45b7-c59f-a481-e053-2995a90ab785

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

doxycycline

Dosage form

CAPSULE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA065055

Marketing category

ANDA

Marketing start

2017-02-14

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