phentermine hydrochloride

Product NDC

0185-0647

11-digit product format

001850647

Labeler code

0185

Product ID

0185-0647_8c3c3331-2016-4a0c-93b3-7198ca1d029e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

phentermine hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Eon Labs, Inc.

Application

ANDA087190

Marketing category

ANDA

Marketing start

1981-06-12

Marketing end

2019-12-31

Substance

PHENTERMINE HYDROCHLORIDE

Active strength

30 mg/1

Pharmacologic classes

Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]

DEA schedule

CIV

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record