up and up temporary minor arthritis pain relief

Product NDC

11673-544

11-digit product format

116730544

Labeler code

11673

Product ID

11673-544_96b8b02b-89e5-4096-baec-4b7126c912df

Type

HUMAN OTC DRUG

Nonproprietary name

Acetaminophen

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Target Corporation

Application

ANDA075077

Marketing category

ANDA

Marketing start

2009-06-23

Marketing end

0000-00-00

Substance

ACETAMINOPHEN

Active strength

650 mg/1

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record