Methylphenidate Hydrochloride

Product NDC

51991-712

11-digit product format

519910712

Labeler code

51991

Product ID

51991-712_6a7bee83-991e-4912-829a-7b81137e2cf3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methylphenidate Hydrochloride

Dosage form

SOLUTION

Route

ORAL

Labeler

Breckenridge Pharmaceutical, Inc.

Application

ANDA091601

Marketing category

ANDA

Marketing start

2010-07-01

Marketing end

2019-06-30

Substance

METHYLPHENIDATE HYDROCHLORIDE

Active strength

5 mg/5mL

Pharmacologic classes

Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]

DEA schedule

CII

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record