Morphine sulfate

Product NDC
71335-0239
11-digit product format
713350239
Labeler code
71335
Product ID
71335-0239_a48a89b3-766b-4a81-a176-89250188a1e4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Morphine sulfate
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA203849
Marketing category
ANDA
Marketing start
2015-10-26
Marketing end
0000-00-00
Substance
MORPHINE SULFATE
Active strength
15 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA schedule
CII
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-0239-07133502390026 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0239-0) 2022-02-090000-00-00NoNoCurrent
71335-0239-17133502390130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0239-1) 2022-02-090000-00-00NoNoCurrent
71335-0239-27133502390260 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0239-2) 2022-02-090000-00-00NoNoCurrent
71335-0239-37133502390390 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0239-3) 2022-02-090000-00-00NoNoCurrent
71335-0239-471335023904120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0239-4) 2022-02-090000-00-00NoNoCurrent
71335-0239-57133502390540 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0239-5) 2022-02-090000-00-00NoNoCurrent
71335-0239-67133502390614 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0239-6) 2022-02-090000-00-00NoNoCurrent
71335-0239-77133502390715 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0239-7) 2022-02-090000-00-00NoNoCurrent
71335-0239-87133502390820 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0239-8) 2022-02-090000-00-00NoNoCurrent
71335-0239-97133502390984 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0239-9) 2022-02-090000-00-00NoNoCurrent