Prednisone

Product NDC
55154-2581
11-digit product format
551542581
Labeler code
55154
Product ID
55154-2581_cdc2b903-5d86-45c1-b97c-2da48445dbdd
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Prednisone
Dosage form
TABLET
Route
ORAL
Labeler
Cardinal Health 107, LLC
Application
ANDA208412
Marketing category
ANDA
Marketing start
2026-03-30
Substance
PREDNISONE
Active strength
20 mg/1
Pharmacologic classes
Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PREDNISONE20 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiVB0R961HZT
Rxcui312615

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
2205d503-be51-445b-bb34-c209cc557b3cProduct name520230105
9492a99d-61c8-491f-9086-1c6a7e98c040Product name620230105
205c2cdd-a63b-cbc9-6bcb-6be6001edf81Product name220170705

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55154-2581-0Prednisone10 in 1 BAGTABLET101
55154-2581-0Prednisone1 in 1 BLISTER PACKTABLET11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
312615predniSONE 20 MG Oral TabletPSNcdc2b903-5d86-45c1-b97c-2da48445dbdd1
312615prednisone 20 MG Oral TabletSCDcdc2b903-5d86-45c1-b97c-2da48445dbdd1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
55154-2581-05515425810010 BLISTER PACK in 1 BAG (55154-2581-0) / 1 TABLET in 1 BLISTER PACK10 blister pack2026-03-30NoNoHistorical