Home NDC 51645-705-10 PlusPharma Extra Strength
Product NDC 51645-705
Requested package NDC 51645-705-10
11-digit product format 516450705
Labeler code 51645
Product ID 51645-705_e8f7b82d-94c5-ab64-e053-2995a90a5910
Type HUMAN OTC DRUG
Nonproprietary name ACETAMINOPHEN
Dosage form TABLET
Route ORAL
Labeler Gemini Pharmaceuticals, Inc. dba Plus Pharma
Application part343
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2006-03-27
Marketing end 2023-05-31
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 0000-00-00
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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ACETAMINOPHEN ACTIVE INGREDIENT 362O9ITL9D PLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG (ACETAMINOPHEN) TABLET [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 3 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D PLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG (ACETAMINOPHEN) TABLET [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 3 POVIDONE INACTIVE INGREDIENT FZ989GH94E PLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG (ACETAMINOPHEN) TABLET [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 3 SODIUM STARCH GLYCOLATE TYPE A CORN INACTIVE INGREDIENT AG9B65PV6B PLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG (ACETAMINOPHEN) TABLET [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 3 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ PLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG (ACETAMINOPHEN) TABLET [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 3 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP PLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG (ACETAMINOPHEN) TABLET [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 3
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 51645-705-10 51645070510 1000 TABLET in 1 BOTTLE, PLASTIC (51645-705-10) 1000 tablet 2006-03-27 2023-05-31 No No Current