Pioglitazone

Product NDC
51079-514
11-digit product format
510790514
Labeler code
51079
Product ID
51079-514_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
2020-01-31
Substance
PIOGLITAZONE HYDROCHLORIDE
Active strength
30 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
51079-514-01EA - Each51079-51461d38a7d-1a8a-4f0d-b1d3-c52e0d4d028312013-02-13
51079-514-20EA - Each51079-514386528b8-ccf4-4f8d-88e2-ee785e2fe80b12013-02-13