Oxybutynin Chloride

Product NDC

70518-0705

11-digit product format

705180705

Labeler code

70518

Product ID

70518-0705_8b4f4971-f422-4940-e053-2995a90ab289

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Oxybutynin Chloride

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA206121

Marketing category

ANDA

Marketing start

2017-08-21

Marketing end

0000-00-00

Substance

OXYBUTYNIN CHLORIDE

Active strength

15 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