MYCOPHENOLATE MOFETIL

Product NDC
72603-751
11-digit product format
726030751
Labeler code
72603
Product ID
72603-751_127eabe2-8386-452a-ad6b-d879e1f2c099
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
mycophenolate mofetil
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Labeler
NorthStar Rx LLC
Application
ANDA218227
Marketing category
ANDA
Marketing start
2026-03-01
Substance
MYCOPHENOLATE MOFETIL
Active strength
200 mg/mL
Pharmacologic classes
Antimetabolite Immunosuppressant [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Source provenance: Browse the complete Orange Book source catalog · source snapshot 42.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A218227-001MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETIL200MG/MLFOR SUSPENSION / ORALAB2024-09-26

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 1 matching rows.

Application-product, TE code table
Application-productTE code
A218227-001AB

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-08-18 06:07:402026-07A218227-001MYCOPHENOLATE MOFETIL200MG/MLFOR SUSPENSION / ORALAB2024-09-26caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A218227-001MYCOPHENOLATE MOFETIL200MG/MLFOR SUSPENSION / ORALAB2024-09-26011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A218227-001MYCOPHENOLATE MOFETIL200MG/MLFOR SUSPENSION / ORALAB2024-09-2631067a03dcf5…
2025-08-23 18:47 UTC2025-08A218227-001MYCOPHENOLATE MOFETIL200MG/MLFOR SUSPENSION / ORALAB2024-09-266a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A218227-001MYCOPHENOLATE MOFETIL200MG/MLFOR SUSPENSION / ORALAB2024-09-26fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A218227-001MYCOPHENOLATE MOFETIL200MG/MLFOR SUSPENSION / ORALAB2024-09-26b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A218227-001MYCOPHENOLATE MOFETIL200MG/MLFOR SUSPENSION / ORALAB2024-09-2603ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A218227-001MYCOPHENOLATE MOFETIL200MG/MLFOR SUSPENSION / ORALAB2024-09-262680178bc6a6…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A218227-001MYCOPHENOLATE MOFETIL200MG/MLFOR SUSPENSION / ORALAB2024-09-26d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A218227-001MYCOPHENOLATE MOFETIL200MG/MLFOR SUSPENSION / ORALAB2024-09-26d06236e962d9…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A218227-001MYCOPHENOLATE MOFETIL200MG/MLFOR SUSPENSION / ORALAB2024-09-26a50c72e98297…

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2026-08-18 06:07:402026-07A218227-001AB1caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A218227-001AB1011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A218227-001AB131067a03dcf5…
2025-08-23 18:47 UTC2025-08A218227-001AB16a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A218227-001AB1fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A218227-001AB1b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A218227-001AB103ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A218227-001AB12680178bc6a6…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A218227-001AB1d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A218227-001AB1d06236e962d9…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A218227-001AB1a50c72e98297…

Additional Listing Data#

Finished product
Yes
Brand name base
MYCOPHENOLATE MOFETIL
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MYCOPHENOLATE MOFETIL200 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
9242ECW6R0Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
311880Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
127eabe2-8386-452a-ad6b-d879e1f2c099Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
04b26d3d-97dc-48db-824b-10b299945382Product name820250224
1aa45098-03f9-4bf8-b28d-2566aa0f7f4bProduct name120250218
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
267b34ba-ace4-4048-9f21-d3c7ac983fc3Product name920210224
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
6084a4f4-5437-c9a5-caec-5361ee075a59Product name120140508
90c5639a-61b0-88d6-ddcf-21888e94869aProduct name120140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72603-751-01MYCOPHENOLATE MOFETIL1 in 1 CARTONPOWDER, FOR SUSPENSION11
72603-751-01MYCOPHENOLATE MOFETIL225 mL in 1 BOTTLEPOWDER, FOR SUSPENSION2251

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72603-751-01ML - Milliliter72603-7519dd03003-cbc7-4f76-8689-0ae73a927aa212026-03-17

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETILNorthStar Rx LLC127eabe2-8386-452a-ad6b-d879e1f2c0992026-01-08Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 218227
application number: ANDA218227
ndc (product): 72603-751
MYCOPHENOLATE MOFETILMYCOPHENOLATE MOFETILAurobindo Pharma Limited20fa7709-a203-481f-aaf4-e98fab1acd0d2025-07-14Boxed warning, Warnings, Adverse reactionsExact identifier
application applno (ANDA): 218227
application number: ANDA218227

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311880mycophenolate mofetil 200 MG in 1 mL Oral SuspensionPSN127eabe2-8386-452a-ad6b-d879e1f2c0991
311880mycophenolate mofetil 200 MG/ML Oral SuspensionSCD127eabe2-8386-452a-ad6b-d879e1f2c0991
311880mycophenolate mofetil 200 MG per 1 ML Oral SuspensionSY127eabe2-8386-452a-ad6b-d879e1f2c0991

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72603-751-01726030751011 BOTTLE in 1 CARTON (72603-751-01) / 225 mL in 1 BOTTLE1 bottle2026-03-01NoNoCurrent