Morphine Sulfate

Product NDC

0409-2029

11-digit product format

004092029

Labeler code

0409

Product ID

0409-2029_4d4f5933-bb5e-43b5-ba72-af44ff5de9b7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

MORPHINE SULFATE

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Hospira, Inc.

Application

NDA019916

Marketing category

NDA

Marketing start

2006-11-28

Marketing end

0000-00-00

Substance

MORPHINE SULFATE

Active strength

1 mg/mL

Pharmacologic classes

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

DEA schedule

CII

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record