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FDA NDA · NDA019872
TYLENOL 8 HR ARTHRITIS PAIN
acetaminophen
Sponsor: KENVUE BRANDS
APPLICATION
NDA019872
TYPE
NDA
ORIGINAL APPROVAL
1994-06-08
LATEST ACTION
2019-01-16
ROUTE
ORAL
DOSAGE FORM
TABLET, EXTENDED RELEASE
MARKETING STATUS
Over-the-counter
Products
TYLENOL · ReferenceOver-the-counter
ACETAMINOPHEN 650MG · TABLET, EXTENDED RELEASE · ORAL
TYLENOL · ReferenceOver-the-counter
ACETAMINOPHEN 650MG · TABLET, EXTENDED RELEASE · ORAL
Approval history
2016-05-05Manufacturing (CMC) · Supplement 43 · standardAP
2013-03-28Manufacturing (CMC) · Supplement 38 · standardAP
2009-09-18Manufacturing (CMC) · Supplement 32AP
2001-02-12Manufacturing (CMC) · Supplement 11 · standardAP
2000-07-25Manufacturing (CMC) · Supplement 10 · standardAP
1995-08-01Manufacturing (CMC) · Supplement 5 · standardAP
1995-07-28Manufacturing (CMC) · Supplement 2 · standardAP
1995-01-05Manufacturing (CMC) · Supplement 3 · standardAP
1994-11-23Manufacturing (CMC) · Supplement 1 · standardAP
1994-06-08Type 3 - New Dosage Form · Original · standardAP
Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.
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