Pioglitazone Hydrochloride

Product NDC
63629-3292
11-digit product format
636293292
Labeler code
63629
Product ID
63629-3292_2901274a-6e9a-49cf-9fa4-27f099a71b3f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pioglitazone Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA200044
Marketing category
ANDA
Marketing start
2013-02-13
Marketing end
0000-00-00
Substance
PIOGLITAZONE HYDROCHLORIDE
Active strength
45 mg/1
Pharmacologic classes
PPAR alpha [CS], PPAR gamma [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor Activity [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63629-3292PIOGLITAZONE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK]12Legacy NDC20241108_89fdabe0-dbd5-442a-ae71-c0281e09760c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-3292-16362932920130 TABLET in 1 BOTTLE (63629-3292-1) 30 tablet2017-01-250000-00-00NoNoCurrent
63629-3292-26362932920290 TABLET in 1 BOTTLE (63629-3292-2) 90 tablet2017-01-250000-00-00NoNoCurrent