Pioglitazone Hydrochloride

Product NDC
68788-6419
11-digit product format
687886419
Labeler code
68788
Product ID
68788-6419_5912cbf0-8db0-4d24-ac8b-8de62580a1b6
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
pioglitazone hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA200044
Marketing category
ANDA
Marketing start
2016-06-14
Marketing end
0000-00-00
Substance
PIOGLITAZONE HYDROCHLORIDE
Active strength
15 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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68788-6419-168788641901100 TABLET in 1 BOTTLE (68788-6419-1) 100 tablet2016-06-140000-00-00NoNoCurrent
68788-6419-36878864190330 TABLET in 1 BOTTLE (68788-6419-3) 30 tablet2016-06-140000-00-00NoNoCurrent
68788-6419-66878864190660 TABLET in 1 BOTTLE (68788-6419-6) 60 tablet2016-06-140000-00-00NoNoCurrent
68788-6419-96878864190990 TABLET in 1 BOTTLE (68788-6419-9) 90 tablet2016-06-140000-00-00NoNoCurrent