Morphine Sulfate

Product NDC

70518-1107

11-digit product format

705181107

Labeler code

70518

Product ID

70518-1107_90232dda-4597-b8d0-e053-2995a90a434a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

MORPHINE SULFATE

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

REMEDYREPACK INC.

Application

NDA019916

Marketing category

NDA

Marketing start

2018-04-11

Marketing end

0000-00-00

Substance

MORPHINE SULFATE

Active strength

5 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