Home NDC 57896-221-10 Extra Strength Pain Relief
Product NDC 57896-221
Requested package NDC 57896-221-10
11-digit product format 578960221
Labeler code 57896
Product ID 57896-221_ed887efa-18b9-7b75-e053-2a95a90adc87
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET
Route ORAL
Labeler Geri-Care Pharmaceutical Corp
Application part343
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 1989-01-01
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 · 1 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 57896-221 57896-221-10 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57896-221 EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) TABLET [GERI-CARE PHARMACEUTICAL CORP] 6 Legacy NDC 20241130_ae00015d-5e5f-4099-ba03-b20bf45ed374.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 57896-221-10 57896022110 1000 TABLET in 1 BOTTLE (57896-221-10) 1000 tablet 2011-11-01 0000-00-00 No No Current