MORPHINE SULFATE

Product NDC

63739-726

11-digit product format

637390726

Labeler code

63739

Product ID

63739-726_1c776dce-7d92-4aa8-b558-89feb537baf6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

MORPHINE SULFATE

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

McKesson Corporation

Application

ANDA076720

Marketing category

ANDA

Marketing start

2015-07-09

Marketing end

0000-00-00

Substance

MORPHINE SULFATE

Active strength

30 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record