Hydromorphone Hydrochloride

Product NDC

51224-102

11-digit product format

512240102

Labeler code

51224

Product ID

51224-102_e907464c-de0d-4fa6-9248-e39b9c558cd5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Hydromorphone Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

TAGI Pharma, Inc.

Application

ANDA076723

Marketing category

ANDA

Marketing start

2012-03-09

Marketing end

2019-08-31

Substance

HYDROMORPHONE HYDROCHLORIDE

Active strength

8 mg/1

Pharmacologic classes

Full Opioid Agonists [MoA],Opioid Agonist [EPC]

DEA schedule

CII

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record