Minocycline Hydrochloride

Product NDC

49999-505

11-digit product format

499990505

Labeler code

49999

Product ID

49999-505_24c4bcfe-5c8f-4058-a294-77e45fc8024f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Minocycline Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA063065

Marketing category

ANDA

Marketing start

2010-10-08

Marketing end

0000-00-00

Substance

MINOCYCLINE HYDROCHLORIDE

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