Morphine sulfate

Product NDC
72162-1790
11-digit product format
721621790
Labeler code
72162
Product ID
72162-1790_f745c084-feeb-4933-912d-8d3ad7702bcf
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
morphine sulfate
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA078761
Marketing category
ANDA
Marketing start
2012-05-11
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
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Morphine sulfate
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MORPHINE SULFATE30 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiX3P646A2J0
Rxcui891888

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
89941d4c-522d-cee0-b273-43cfa7ef6d35Product name420250516
f15f9e76-db42-8a50-218a-5ef5affa58daProduct name420240216
944b0689-73f4-6a2f-c654-1180896353c0Product name420220210
67e166c6-23d4-4709-b77d-5ca6182dcae0Product name120180830
c573a64c-fe17-2eac-fbcb-788868b4ff6bProduct name920180619
7c1819cf-69a0-41dc-aeaa-a820729bc959Product name120170406
7a68fc31-10e5-df04-67e0-3a613a2d4d2eProduct name520161114
175682a8-c657-45a2-9dfb-c565306b03c8Product name120160112
b73dadd0-1b4a-4f88-956f-a2be216c8fadProduct name120151123
4c272b1c-87fc-ebc0-994d-ac28b1e0416eProduct name120140508
7a537f54-d322-5e54-a3a2-035d3e21c3c6Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72162-1790-1Morphine sulfate100 in 1 BOTTLETABLET, FILM COATED, EXTENDED RE100103
72162-1790-3Morphine sulfate30 in 1 BOTTLETABLET, FILM COATED, EXTENDED RE30103
72162-1790-6Morphine sulfate60 in 1 BOTTLETABLET, FILM COATED, EXTENDED RE60103
72162-1790-9Morphine sulfate90 in 1 BOTTLETABLET, FILM COATED, EXTENDED RE90103

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72162-1790-1EA - Each72162-17903abedf21-c382-4b96-90c7-39f63aeb848412023-10-16
72162-1790-3EA - Each72162-17903493c580-61cf-4e7d-9576-5d8c1459cf8b12023-10-16
72162-1790-6EA - Each72162-1790fc55b180-add9-40bd-90e5-c817441855b412023-10-16
72162-1790-9EA - Each72162-1790ec6cb3f0-c89e-495a-b46d-c8941e30b6d812023-10-16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72162-1790MORPHINE SULFATE TABLET, FILM COATED, EXTENDED RELEASE [BRYANT RANCH PREPACK]103Current NDC, 4 package rows20240821_20af0f0e-45cc-4795-97ef-90b659575b34.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
891888morphine sulfate 30 MG Extended Release Oral TabletPSN20af0f0e-45cc-4795-97ef-90b659575b34103
891888morphine sulfate 30 MG Extended Release Oral TabletSCD20af0f0e-45cc-4795-97ef-90b659575b34103
891888MS 30 MG Extended Release Oral TabletSY20af0f0e-45cc-4795-97ef-90b659575b34103

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
72162-1790-172162179001100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1790-1) 2012-05-11NoNoHistorical
72162-1790-37216217900330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1790-3) 2012-05-11NoNoHistorical
72162-1790-67216217900660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1790-6) 2012-05-11NoNoHistorical
72162-1790-97216217900990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1790-9) 2012-05-11NoNoHistorical