Morphine sulfate

Product NDC
72162-1793
11-digit product format
721621793
Labeler code
72162
Product ID
72162-1793_52d882e9-36da-454b-b16b-a3522258e0be
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
60 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 SULFATE60 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiX3P646A2J0
Rxcui891893

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
72162-1793-1Morphine sulfate100 in 1 BOTTLETABLET, FILM COATED, EXTENDED RE100105
72162-1793-3Morphine sulfate30 in 1 BOTTLETABLET, FILM COATED, EXTENDED RE30105
72162-1793-6Morphine sulfate60 in 1 BOTTLETABLET, FILM COATED, EXTENDED RE60105
72162-1793-9Morphine sulfate90 in 1 BOTTLETABLET, FILM COATED, EXTENDED RE90105

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72162-1793-1EA - Each72162-1793a350f140-a0a9-49d5-b353-66bbd69616b912023-10-16
72162-1793-3EA - Each72162-1793dabfc9f2-72ba-4557-ac5a-7aaefbc67ec512023-10-16
72162-1793-6EA - Each72162-1793521561c1-6243-4a5e-8c95-9d20d72d9f5a12023-10-16
72162-1793-9EA - Each72162-1793be71afab-d0b0-4b94-80fb-141a548cf83f12023-10-16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72162-1793MORPHINE SULFATE TABLET, FILM COATED, EXTENDED RELEASE [BRYANT RANCH PREPACK]105Current NDC, 4 package rows20240927_7f65fa22-c3fc-4413-8a07-2c6be621b7bf.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
891893morphine sulfate 60 MG Extended Release Oral TabletPSN7f65fa22-c3fc-4413-8a07-2c6be621b7bf105
891893morphine sulfate 60 MG Extended Release Oral TabletSCD7f65fa22-c3fc-4413-8a07-2c6be621b7bf105
891893MS 60 MG Extended Release Oral TabletSY7f65fa22-c3fc-4413-8a07-2c6be621b7bf105

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
72162-1793-172162179301100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1793-1) 2012-05-11NoNoHistorical
72162-1793-37216217930330 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1793-3) 2012-05-11NoNoHistorical
72162-1793-67216217930660 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1793-6) 2012-05-11NoNoHistorical
72162-1793-97216217930990 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1793-9) 2012-05-11NoNoHistorical