Prednisone

Product NDC
66336-094
11-digit product format
663360094
Labeler code
66336
Product ID
66336-094_b8c45bf4-669b-434a-a646-9891555c263d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Prednisone
Dosage form
TABLET
Route
ORAL
Labeler
Dispensing Solutions, Inc.
Application
ANDA040392
Marketing category
ANDA
Marketing start
2003-02-12
Marketing end
0000-00-00
Substance
PREDNISONE
Active strength
20 mg/1
Pharmacologic classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66336-094-152019-11-27C16284748780-19855d018-ea7a-cd31-e053-dbdaa90ab51aPredniSONE TABLETS, USP 20 mg
66336-094-212019-11-27C16284748780-19855d018-ea7a-cd31-e053-dbdaa90ab51aPredniSONE TABLETS, USP 20 mg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66336-094-15Prednisone15 in 1 BOTTLE, PLASTICTABLET153
66336-094-21Prednisone21 in 1 BOTTLE, PLASTICTABLET213

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66336-094-21EA - Each66336-094b782e53d-7512-4b03-8507-121579d0743c12013-04-01

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PREDNISONEACTIVE INGREDIENTVB0R961HZTPREDNISONE TABLET [DISPENSING SOLUTIONS, INC.]3
PREDNISONEACTIVE MOIETYVB0R961HZTPREDNISONE TABLET [DISPENSING SOLUTIONS, INC.]3
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UPREDNISONE TABLET [DISPENSING SOLUTIONS, INC.]3
FD&C YELLOW NO. 6INACTIVE INGREDIENTH77VEI93A8PREDNISONE TABLET [DISPENSING SOLUTIONS, INC.]3
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XPREDNISONE TABLET [DISPENSING SOLUTIONS, INC.]3
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30PREDNISONE TABLET [DISPENSING SOLUTIONS, INC.]3
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2PREDNISONE TABLET [DISPENSING SOLUTIONS, INC.]3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66336-094PREDNISONE TABLET [DISPENSING SOLUTIONS, INC.]3Legacy NDC, 2 package rows20130316_9fcd7814-1363-4218-92c6-b0f732795897.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
312615predniSONE 20 MG Oral TabletPSN9fcd7814-1363-4218-92c6-b0f7327958973
312615prednisone 20 MG Oral TabletSCD9fcd7814-1363-4218-92c6-b0f7327958973

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
66336-094-156633600941515 in 1 BOTTLE, PLASTICHistorical
66336-094-216633600942121 in 1 BOTTLE, PLASTICHistorical