Risedronate Sodium

Product NDC
65862-517
11-digit product format
658620517
Labeler code
65862
Product ID
65862-517_9488209f-f3ad-4726-be89-f6a7e59e6885
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Risedronate Sodium
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Aurobindo Pharma Limited
Application
ANDA200296
Marketing category
ANDA
Marketing start
2015-11-30
Substance
RISEDRONATE SODIUM
Active strength
5 mg/1
Pharmacologic classes
Bisphosphonate [EPC], Diphosphonates [CS]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
RISEDRONATE SODIUM5 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiOFG5EXG60L
Rxcui905024, 905032, 905041, 905092, 905100

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dc99ed49-98e9-42a6-aef0-a6dc585a6a09Product name420191002
a51ae56f-109a-47a0-9ce1-2b825be8c01bProduct name520190614

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65862-517-10Risedronate Sodium10 in 1 BLISTER PACKTABLET, FILM COATED109
65862-517-22Risedronate Sodium2000 in 1 BOTTLETABLET, FILM COATED20009
65862-517-30Risedronate Sodium30 in 1 BOTTLETABLET, FILM COATED309
65862-517-78Risedronate Sodium10 in 1 CARTONTABLET, FILM COATED109

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
65862-517-30EA - Each65862-517340a8495-0089-4048-9a0c-9072b19286af12016-01-13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65862-517RISEDRONATE SODIUM TABLET, FILM COATED [AUROBINDO PHARMA LIMITED]8Current NDC, Legacy NDC, 4 package rows20240202_89896dfe-f69d-4cb3-bb71-7a7c611071fa.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
905100{12 (risedronate sodium 35 MG Oral Tablet) } PackGPCK89896dfe-f69d-4cb3-bb71-7a7c611071fa9
905092{4 (risedronate sodium 35 MG Oral Tablet) } PackGPCK89896dfe-f69d-4cb3-bb71-7a7c611071fa9
905032risedronate sodium 30 MG Oral TabletPSN89896dfe-f69d-4cb3-bb71-7a7c611071fa9
905100risedronate sodium 35 MG (12) Oral Tablet PackPSN89896dfe-f69d-4cb3-bb71-7a7c611071fa9
905092risedronate sodium 35 MG (4) Oral Tablet PackPSN89896dfe-f69d-4cb3-bb71-7a7c611071fa9
905024risedronate sodium 35 MG Oral TabletPSN89896dfe-f69d-4cb3-bb71-7a7c611071fa9
905041risedronate sodium 5 MG Oral TabletPSN89896dfe-f69d-4cb3-bb71-7a7c611071fa9
905032risedronate sodium 30 MG Oral TabletSCD89896dfe-f69d-4cb3-bb71-7a7c611071fa9
905024risedronate sodium 35 MG Oral TabletSCD89896dfe-f69d-4cb3-bb71-7a7c611071fa9
905041risedronate sodium 5 MG Oral TabletSCD89896dfe-f69d-4cb3-bb71-7a7c611071fa9
905100risedronate sodium 35 MG Oral Tablet, 12 Week PackSY89896dfe-f69d-4cb3-bb71-7a7c611071fa9
905092risedronate sodium 35 MG Oral Tablet, 4 Week PackSY89896dfe-f69d-4cb3-bb71-7a7c611071fa9

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
65862-517-106586205171010 in 1 BLISTER PACKHistorical
65862-517-196586205171910000 TABLET, FILM COATED in 1 BAG (65862-517-19)30-NOV-15Current
65862-517-22658620517222000 TABLET, FILM COATED in 1 BOTTLE (65862-517-22) 2015-11-300000-00-00NoNoCurrent
65862-517-306586205173030 TABLET, FILM COATED in 1 BOTTLE (65862-517-30) 2015-11-300000-00-00NoNoCurrent
65862-517-786586205177810 BLISTER PACK in 1 CARTON (65862-517-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-517-10) 10 blister pack2015-11-300000-00-00NoNoCurrent