Home NDC 71679-031-00 Extra Strenghth Acetaminophen
Product NDC 71679-031
Requested package NDC 71679-031-00
11-digit product format 716790031
Labeler code 71679
Product ID 71679-031_eeb7359e-ed8e-1e90-e053-2a95a90a48d9
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET
Route ORAL
Labeler Health Pharma USA LLC
Application part343
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2017-07-31
Marketing end 0000-00-00
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 71679-031 71679-031-00 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 71679-031 71679-031-00 D Discontinued by firm excluded / ndc_excluded.zip f5e01cc5f278…a2eaf40c39c3…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71679-031-00 71679003100 1 BAG in 1 BOX (71679-031-00) > 29090 TABLET in 1 BAG 1 bag 2017-07-31 0000-00-00 No No Current