Doxycycline hyclate

Product NDC

68382-211

11-digit product format

683820211

Labeler code

68382

Product ID

68382-211_4d995c1e-1d4c-454a-94da-39c1b28760f7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Doxycycline hyclate

Dosage form

TABLET

Route

ORAL

Labeler

Zydus Pharmaceuticals (USA) Inc.

Application

ANDA207773

Marketing category

ANDA

Marketing start

2018-04-02

Marketing end

0000-00-00

Substance

DOXYCYCLINE HYCLATE

Active strength

100 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record