Oxybutynin Chloride

Product NDC

43063-145

11-digit product format

430630145

Labeler code

43063

Product ID

43063-145_7d3ab634-7cad-36af-e053-2a91aa0af8e5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

oxybutynin chloride

Dosage form

TABLET

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA075079

Marketing category

ANDA

Marketing start

1997-10-31

Marketing end

0000-00-00

Substance

OXYBUTYNIN CHLORIDE

Active strength

5 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record