Pioglitazone

Product NDC

70518-2324

11-digit product format

705182324

Labeler code

70518

Product ID

70518-2324_9356cd5d-9934-cd08-e053-2995a90a55d2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

pioglitazone

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA078670

Marketing category

ANDA

Marketing start

2019-09-24

Marketing end

0000-00-00

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

2020-12-31

Current FDA listing

Historical FDA.report record