Childrens Ibuprofen Oral Suspension

Product NDC

0121-1820

11-digit product format

001211820

Labeler code

0121

Product ID

0121-1820_aa8231ce-0c8a-09d4-e053-2995a90a6bd0

Type

HUMAN OTC DRUG

Nonproprietary name

Ibuprofen

Dosage form

SUSPENSION

Route

ORAL

Labeler

Pharmaceutical Associates, Inc.

Application

ANDA074916

Marketing category

ANDA

Marketing start

1999-04-30

Marketing end

0000-00-00

Substance

IBUPROFEN

Active strength

100 mg/10mL

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record