Pioglitazone

Product NDC
68788-7989
11-digit product format
687887989
Labeler code
68788
Product ID
68788-7989_743b22a3-03e4-4a8c-808e-379297058262
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Pioglitazone
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals, Inc.
Application
ANDA077210
Marketing category
ANDA
Marketing start
2021-08-27
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
68788-7989-168788798901100 TABLET in 1 BOTTLE (68788-7989-1) 100 tablet2021-08-270000-00-00NoNoCurrent
68788-7989-36878879890330 TABLET in 1 BOTTLE (68788-7989-3) 30 tablet2021-08-270000-00-00NoNoCurrent
68788-7989-66878879890660 TABLET in 1 BOTTLE (68788-7989-6) 60 tablet2021-08-270000-00-00NoNoCurrent
68788-7989-96878879890990 TABLET in 1 BOTTLE (68788-7989-9) 90 tablet2021-08-270000-00-00NoNoCurrent