Mycophenolate Mofetil

Product NDC
0781-2067
11-digit product format
007812067
Labeler code
0781
Product ID
0781-2067_8d255117-cfa8-4893-8e2e-945eee7b12c4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Mycophenolate Mofetil
Dosage form
CAPSULE
Route
ORAL
Labeler
Sandoz Inc
Application
ANDA065379
Marketing category
ANDA
Marketing start
2008-10-15
Substance
MYCOPHENOLATE MOFETIL
Active strength
250 mg/1
Pharmacologic classes
Antimetabolite Immunosuppressant [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Mycophenolate Mofetil
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MYCOPHENOLATE MOFETIL250 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9242ECW6R0
Rxcui199058, 200060

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
04b26d3d-97dc-48db-824b-10b299945382Product name820250224
1aa45098-03f9-4bf8-b28d-2566aa0f7f4bProduct name120250218
267b34ba-ace4-4048-9f21-d3c7ac983fc3Product name920210224

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0781-2067-012023-08-02C16284748780-10191ceaa-6637-198a-e063-dbdaa90aec3eThese highlights do not include all the information needed to use MYCOPHENOLATE MOFETIL safely and effectively. See full prescribing information for MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL capsules, for oral use MYCOPHENOLATE MOFETIL tablets, for oral use Initial U.S. Approval: 1995
0781-2067-052023-08-02C16284748780-10191ceaa-6637-198a-e063-dbdaa90aec3eThese highlights do not include all the information needed to use MYCOPHENOLATE MOFETIL safely and effectively. See full prescribing information for MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL capsules, for oral use MYCOPHENOLATE MOFETIL tablets, for oral use Initial U.S. Approval: 1995
0781-2067-722023-08-02C16284748780-10191ceaa-6637-198a-e063-dbdaa90aec3eThese highlights do not include all the information needed to use MYCOPHENOLATE MOFETIL safely and effectively. See full prescribing information for MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL capsules, for oral use MYCOPHENOLATE MOFETIL tablets, for oral use Initial U.S. Approval: 1995
0781-2067-892023-08-02C16284748780-10191ceaa-6637-198a-e063-dbdaa90aec3eThese highlights do not include all the information needed to use MYCOPHENOLATE MOFETIL safely and effectively. See full prescribing information for MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL capsules, for oral use MYCOPHENOLATE MOFETIL tablets, for oral use Initial U.S. Approval: 1995
0781-2067-012023-07-28C16284748780-10191ceaa-6637-198a-e063-dbdaa90aec3eThese highlights do not include all the information needed to use MYCOPHENOLATE MOFETIL safely and effectively. See full prescribing information for MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL capsules, for oral use MYCOPHENOLATE MOFETIL tablets, for oral use Initial U.S. Approval: 1995
0781-2067-052023-07-28C16284748780-10191ceaa-6637-198a-e063-dbdaa90aec3eThese highlights do not include all the information needed to use MYCOPHENOLATE MOFETIL safely and effectively. See full prescribing information for MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL capsules, for oral use MYCOPHENOLATE MOFETIL tablets, for oral use Initial U.S. Approval: 1995
0781-2067-722023-07-28C16284748780-10191ceaa-6637-198a-e063-dbdaa90aec3eThese highlights do not include all the information needed to use MYCOPHENOLATE MOFETIL safely and effectively. See full prescribing information for MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL capsules, for oral use MYCOPHENOLATE MOFETIL tablets, for oral use Initial U.S. Approval: 1995
0781-2067-892023-07-28C16284748780-10191ceaa-6637-198a-e063-dbdaa90aec3eThese highlights do not include all the information needed to use MYCOPHENOLATE MOFETIL safely and effectively. See full prescribing information for MYCOPHENOLATE MOFETIL. MYCOPHENOLATE MOFETIL capsules, for oral use MYCOPHENOLATE MOFETIL tablets, for oral use Initial U.S. Approval: 1995

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0781-2067-01Mycophenolate Mofetil100 in 1 BOTTLECAPSULE10020
0781-2067-05Mycophenolate Mofetil500 in 1 BOTTLECAPSULE50020
0781-2067-72Mycophenolate Mofetil120 in 1 BOTTLECAPSULE12020
0781-2067-89Mycophenolate Mofetil12 in 1 CARTONCAPSULE1220

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0781-2067-01EA - Each0781-206705dbc7ef-a774-4a3f-a932-887891d2d16812012-07-24
0781-2067-05EA - Each0781-2067c20bb4d1-a4bc-48a9-ac60-043c44043f5c12012-07-24
0781-2067-89EA - Each0781-20675a286ba1-b876-41a1-a5cd-ca3e07cd81ad12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MYCOPHENOLATE MOFETILACTIVE INGREDIENT9242ECW6R0MYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9
MYCOPHENOLIC ACIDACTIVE MOIETYHU9DX48N0TMYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9
ALCOHOLINACTIVE INGREDIENT3K9958V90MMYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9
AMMONIAINACTIVE INGREDIENT5138Q19F1XMYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9
BUTYL ALCOHOLINACTIVE INGREDIENT8PJ61P6TS3MYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48MYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9
FD&C BLUE NO. 2INACTIVE INGREDIENTL06K8R7DQKMYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9
FERROSOFERRIC OXIDEINACTIVE INGREDIENTXM0M87F357MYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9
GELATININACTIVE INGREDIENT2G86QN327LMYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9
ISOPROPYL ALCOHOLINACTIVE INGREDIENTND2M416302MYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30MYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9
POTASSIUM HYDROXIDEINACTIVE INGREDIENTWZH3C48M4TMYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9
POVIDONE K90INACTIVE INGREDIENTRDH86HJV5ZMYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3MYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9
SHELLACINACTIVE INGREDIENT46N107B71OMYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJMYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPMYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9
WATERINACTIVE INGREDIENT059QF0KO0RMYCOPHENOLATE MOFETIL CAPSULE [SANDOZ INC]9

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0781-2067MYCOPHENOLATE MOFETIL CAPSULE MYCOPHENOLATE MOFETIL TABLET, FILM COATED [SANDOZ INC]18Current NDC, Legacy NDC, 4 package rows20230803_99b2eb58-8d14-48fc-bbe1-aacb711a783e.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
199058mycophenolate mofetil 250 MG Oral CapsulePSN99b2eb58-8d14-48fc-bbe1-aacb711a783e20
200060mycophenolate mofetil 500 MG Oral TabletPSN99b2eb58-8d14-48fc-bbe1-aacb711a783e20
199058mycophenolate mofetil 250 MG Oral CapsuleSCD99b2eb58-8d14-48fc-bbe1-aacb711a783e20
200060mycophenolate mofetil 500 MG Oral TabletSCD99b2eb58-8d14-48fc-bbe1-aacb711a783e20

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0781-2067-0100781206701100 CAPSULE in 1 BOTTLE (0781-2067-01) 100 capsule2008-10-150000-00-00NoNoCurrent
0781-2067-0500781206705500 CAPSULE in 1 BOTTLE (0781-2067-05) 500 capsule2008-10-150000-00-00NoNoCurrent
0781-2067-7200781206772120 CAPSULE in 1 BOTTLE (0781-2067-72) 120 capsule2008-10-150000-00-00NoNoCurrent
0781-2067-890078120678912 CAPSULE in 1 CARTON (0781-2067-89) 12 capsule2008-10-150000-00-00NoNoCurrent