oxybutynin chloride

Product NDC

70518-0158

11-digit product format

705180158

Labeler code

70518

Product ID

70518-0158_8233246f-796e-eb9b-e053-2991aa0a688b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxybutynin chloride

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA207138

Marketing category

ANDA

Marketing start

2017-01-19

Marketing end

0000-00-00

Substance

OXYBUTYNIN CHLORIDE

Active strength

10 mg/1

Pharmacologic classes

Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record