Doxycycline Hyclate

Product NDC

69235-320

11-digit product format

692350320

Labeler code

69235

Product ID

69235-320_7e252f72-19a6-4768-b30b-80eb6fbd3d00

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Doxycycline Hyclate

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

MHC Pharma, LLC

Application

ANDA062505

Marketing category

ANDA

Marketing start

1984-09-11

Marketing end

2019-05-31

Substance

DOXYCYCLINE HYCLATE

Active strength

100 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