Pioglitazone

Product NDC
51079-515
11-digit product format
510790515
Labeler code
51079
Product ID
51079-515_7d7c9874-0673-255a-e053-2991aa0ab6ca
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
pioglitazone
Dosage form
TABLET
Route
ORAL
Labeler
Mylan Institutional Inc.
Application
ANDA076801
Marketing category
ANDA
Marketing start
2012-09-06
Marketing end
2019-10-31
Substance
PIOGLITAZONE HYDROCHLORIDE
Active strength
45 mg/1
Pharmacologic classes
Peroxisome Proliferator-activated Receptor Activity [MoA],PPAR alpha [CS],PPAR gamma [CS],Thiazolidinedione [EPC],Thiazolidinediones [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC],Peroxisome Proliferator Receptor gamma Agonist [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51079-515-01EA - Each51079-5151baa3c14-7c12-4f5e-ad86-ac4ea63fefea12013-02-13
51079-515-20EA - Each51079-5159cb8d951-31c2-4c31-af2e-61571e90fa7112013-02-13