sirolimus

Product NDC
72162-2641
11-digit product format
721622641
Labeler code
72162
Product ID
72162-2641_71b9e046-12b4-4224-ab7a-ae65b34b5c1c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
sirolimus
Dosage form
SOLUTION
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA216728
Marketing category
ANDA
Marketing start
2023-01-19
Substance
SIROLIMUS
Active strength
1 mg/mL
Pharmacologic classes
Decreased Immunologic Activity [PE], Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA], mTOR Inhibitor Immunosuppressant [EPC], mTOR Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SIROLIMUS1 mg/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiW36ZG6FT64
Rxcui314230

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e68235d1-1e8b-9d8c-fddb-764b8b692c25Product name720250331
9344cc31-0398-4e2f-a65e-a24a0de47fc4Product name120230103
741e13fe-61d8-4a4c-8c27-eb206b28f1bfProduct name120220613

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72162-2641-6sirolimus1 in 1 CARTONSOLUTION1100
72162-2641-6sirolimus60 mL in 1 BOTTLE, GLASSSOLUTION60100

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
314230sirolimus 1 MG in 1 mL Oral SolutionPSNf9843d49-0e16-4427-9cea-9f66f32b97f7100
314230sirolimus 1 MG/ML Oral SolutionSCDf9843d49-0e16-4427-9cea-9f66f32b97f7100
314230sirolimus 1 MG per 1 ML Oral SolutionSYf9843d49-0e16-4427-9cea-9f66f32b97f7100

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
72162-2641-6721622641061 BOTTLE, GLASS in 1 CARTON (72162-2641-6) / 60 mL in 1 BOTTLE, GLASS2026-05-06NoNoHistorical