Morphine sulfate

Product NDC
71335-0605
11-digit product format
713350605
Labeler code
71335
Product ID
71335-0605_e34292d1-deb6-4d06-999f-dc3f3f358272
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
30 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA schedule
CII
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-0605-07133506050040 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0605-0) 2016-01-050000-00-00NoNoCurrent
71335-0605-17133506050130 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0605-1) 2016-01-050000-00-00NoNoCurrent
71335-0605-27133506050260 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0605-2) 2016-01-050000-00-00NoNoCurrent
71335-0605-37133506050390 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0605-3) 2016-01-050000-00-00NoNoCurrent
71335-0605-471335060504120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0605-4) 2016-01-050000-00-00NoNoCurrent
71335-0605-571335060505100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0605-5) 2016-01-050000-00-00NoNoCurrent
71335-0605-6713350605065 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0605-6) 2016-01-050000-00-00NoNoCurrent
71335-0605-77133506050715 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0605-7) 2016-01-050000-00-00NoNoCurrent
71335-0605-87133506050820 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0605-8) 2016-01-050000-00-00NoNoCurrent
71335-0605-97133506050926 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0605-9) 2016-01-050000-00-00NoNoCurrent