Docusate Sodium

Product NDC

53329-660

11-digit product format

533290660

Labeler code

53329

Product ID

53329-660_5f248cb7-b9f5-00b5-e053-2a91aa0a1a12

Type

HUMAN OTC DRUG

Nonproprietary name

Docusate Sodium

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Medline Industries, Inc.

Application

part334

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2013-01-16

Marketing end

0000-00-00

Substance

DOCUSATE SODIUM

Active strength

100 mg/1

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record