FDA.reportPublic FDA data

Pioglitazone

Product NDC
70518-2609
11-digit product format
705182609
Labeler code
70518
Product ID
70518-2609_4a79b87a-fc62-6b91-e063-6294a90aed48
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pioglitazone
Dosage form
TABLET
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA200268
Marketing category
ANDA
Marketing start
2020-03-02
Substance
PIOGLITAZONE HYDROCHLORIDE
Active strength
15 mg/1
Pharmacologic classes
Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA], Peroxisome Proliferator-activated Receptor gamma Agonists [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PIOGLITAZONE HYDROCHLORIDE15 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiJQT35NPK6C
Rxcui317573

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e11f0f31-8914-938f-521e-037b6de27c13Product name520210621
3e9b6ece-066b-2ac3-28f7-5e13060e5934Product name220151109
0d79b284-47e8-e90c-f249-892b9b251003Product name120140508
7611093e-8875-33d4-9e3c-f48c7e3af1e8Product name120140508
ac29cd77-922c-d25a-f8ad-66a8692935c5Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70518-2609-02022-01-31C16284748780-1d6a99b39-e495-a426-e053-dadaa90af4c2These highlights do not include all the information needed to use PIOGLITAZONE TABLETS safely and effectively. See full prescribing information for PIOGLITAZONE TABLETS. PIOGLITAZONE tablets, for oral use Initial U.S. Approval: 1999
70518-2609-02022-01-28C16284748780-1d6a99b39-e495-a426-e053-dadaa90af4c2These highlights do not include all the information needed to use PIOGLITAZONE TABLETS safely and effectively. See full prescribing information for PIOGLITAZONE TABLETS. PIOGLITAZONE tablets, for oral use Initial U.S. Approval: 1999

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70518-2609-0Pioglitazone90 in 1 BOTTLE, PLASTICTABLET909

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70518-2609PIOGLITAZONE TABLET [REMEDYREPACK INC.]7Current NDC, Legacy NDC, 1 package rows20250322_3a9f6777-9b4f-482a-aa4e-4900f9d35b8e.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
317573pioglitazone 15 MG Oral TabletPSN3a9f6777-9b4f-482a-aa4e-4900f9d35b8e9
317573pioglitazone 15 MG Oral TabletSCD3a9f6777-9b4f-482a-aa4e-4900f9d35b8e9
317573pioglitazone (as pioglitazone hydrochloride) 15 MG Oral TabletSY3a9f6777-9b4f-482a-aa4e-4900f9d35b8e9

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70518-2609-07051826090090 TABLET in 1 BOTTLE, PLASTIC (70518-2609-0) 90 tablet2020-03-020000-00-00NoNoCurrent