Morphine Sulfate

Product NDC

70408-359

11-digit product format

704080359

Labeler code

70408

Product ID

70408-359_582a61e9-7fec-4c66-b3a5-1e8d0a9b71f8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Morphine Sulfate

Dosage form

SOLUTION

Route

ORAL

Labeler

Nostrum Laboratories, Inc.

Application

ANDA201011

Marketing category

ANDA

Marketing start

2014-02-05

Marketing end

0000-00-00

Substance

MORPHINE SULFATE

Active strength

20 mg/5mL

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