Minocycline Hydrochloride

Product NDC

21695-693

11-digit product format

216950693

Labeler code

21695

Product ID

21695-693_a74f9195-8a43-428f-9262-a41313165e0a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Minocycline Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Rebel Distributors Corp.

Application

ANDA065062

Marketing category

ANDA

Marketing start

2000-11-30

Marketing end

0000-00-00

Substance

MINOCYCLINE HYDROCHLORIDE

Active strength

50 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record