Pioglitazone Hydrochloride

Product NDC

70518-1882

11-digit product format

705181882

Labeler code

70518

Product ID

70518-1882_82602de1-e102-0b7c-e053-2991aa0a0b64

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Pioglitazone Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA200044

Marketing category

ANDA

Marketing start

2019-02-19

Marketing end

0000-00-00

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

2020-12-31

Current FDA listing

Historical FDA.report record