FDA.reportPublic FDA data

SAXAGLIPTIN

Product NDC
68462-726
11-digit product format
684620726
Labeler code
68462
Product ID
68462-726_4d1a25c6-4ffc-4714-98a9-c4dcb2049d6d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
SAXAGLIPTIN
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Glenmark Pharmaceuticals Inc., USA
Application
ANDA205994
Marketing category
ANDA
Marketing start
2023-07-31
Substance
SAXAGLIPTIN HYDROCHLORIDE
Active strength
2.5 mg/1
Pharmacologic classes
Dipeptidyl Peptidase 4 Inhibitor [EPC], Dipeptidyl Peptidase 4 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
SAXAGLIPTIN
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SAXAGLIPTIN HYDROCHLORIDE2.5 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiZ8J84YIX6L
Rxcui858036, 858042

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
08b60e13-e5d0-74ca-b5a8-e6df9cb1dca0Product name220240829
f5a91c01-b85a-4a74-4259-0bddd9950e83Product name220240828
1dc427fa-8c3b-4309-981e-ea1ff01326e5Product name120190731
85b4e38c-4488-4e48-919e-244e107d9bd9Product name220190731

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68462-726-05SAXAGLIPTIN500 in 1 BOTTLETABLET, FILM COATED5002
68462-726-30SAXAGLIPTIN30 in 1 BOTTLETABLET, FILM COATED302
68462-726-90SAXAGLIPTIN90 in 1 BOTTLETABLET, FILM COATED902

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68462-726-30EA - Each68462-726ec3e3b24-14bd-4d0c-949f-753ee21214de12023-09-05
68462-726-90EA - Each68462-7261865826c-6e65-419b-8261-44ef1b7734b912023-09-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68462-726SAXAGLIPTIN TABLET, FILM COATED [GLENMARK PHARMACEUTICALS INC., USA]1Current NDC, 3 package rows20230808_e286ffd4-c598-47fb-af06-2e15f7e6f99f.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
858042sAXagliptin 2.5 MG Oral TabletPSNe286ffd4-c598-47fb-af06-2e15f7e6f99f2
858036sAXagliptin 5 MG Oral TabletPSNe286ffd4-c598-47fb-af06-2e15f7e6f99f2
858042saxagliptin 2.5 MG Oral TabletSCDe286ffd4-c598-47fb-af06-2e15f7e6f99f2
858036saxagliptin 5 MG Oral TabletSCDe286ffd4-c598-47fb-af06-2e15f7e6f99f2
858042saxagliptin 2.5 MG (as saxagliptin HCl, anhydrous 2.79 MG) Oral TabletSYe286ffd4-c598-47fb-af06-2e15f7e6f99f2
858036saxagliptin 5 MG (as saxagliptin HCl, anhydrous 5.58 MG) Oral TabletSYe286ffd4-c598-47fb-af06-2e15f7e6f99f2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
68462-726-0568462072605500 TABLET, FILM COATED in 1 BOTTLE (68462-726-05) 2023-07-31NoNoHistorical
68462-726-306846207263030 TABLET, FILM COATED in 1 BOTTLE (68462-726-30) 2023-07-31NoNoHistorical
68462-726-906846207269090 TABLET, FILM COATED in 1 BOTTLE (68462-726-90) 2023-07-31NoNoHistorical