DILAUDID

Product NDC

59011-458

11-digit product format

590110458

Labeler code

59011

Product ID

59011-458_0cc002bd-a7e7-0cd0-bf27-678460984ad5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

HYDROMORPHONE HYDROCHLORIDE

Dosage form

TABLET

Route

ORAL

Labeler

Purdue Pharma LP

Application

NDA019892

Marketing category

NDA

Marketing start

1956-01-01

Marketing end

0000-00-00

Substance

HYDROMORPHONE HYDROCHLORIDE

Active strength

8 mg/1

Pharmacologic classes

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

DEA schedule

CII

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record