Home NDC 51645-706 PlusPharma Extra Strength
Product NDC 51645-706
11-digit product format 516450706
Labeler code 51645
Product ID 51645-706_e8f7bed1-18ee-b041-e053-2a95a90a087f
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 2023-12-31
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 · 36 matching rows.
View current auxiliary records. · View the auxiliary file history.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# 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] 4 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D PLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG (ACETAMINOPHEN) TABLET [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 4 POVIDONE INACTIVE INGREDIENT FZ989GH94E PLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG (ACETAMINOPHEN) TABLET [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 4 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] 4 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ PLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG (ACETAMINOPHEN) TABLET [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 4 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP PLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG (ACETAMINOPHEN) TABLET [GEMINI PHARMACEUTICALS, INC. DBA PLUS PHARMA] 4 ACETAMINOPHEN ACTIVE INGREDIENT 362O9ITL9D PLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG (ACETAMINOPHEN) TABLET [PROFICIENT RX LP] 1 ACETAMINOPHEN ACTIVE INGREDIENT 362O9ITL9D ACETAMINOPHEN TABLET [REBEL DISTRIBUTORS CORP] 1 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D PLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG (ACETAMINOPHEN) TABLET [PROFICIENT RX LP] 1 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D ACETAMINOPHEN TABLET [REBEL DISTRIBUTORS CORP] 1 CROSPOVIDONE INACTIVE INGREDIENT 68401960MK ACETAMINOPHEN TABLET [REBEL DISTRIBUTORS CORP] 1 POVIDONE INACTIVE INGREDIENT FZ989GH94E ACETAMINOPHEN TABLET [REBEL DISTRIBUTORS CORP] 1 POVIDONES INACTIVE INGREDIENT FZ989GH94E PLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG (ACETAMINOPHEN) TABLET [PROFICIENT RX LP] 1 SODIUM STARCH GLYCOLATE TYPE A CORN INACTIVE INGREDIENT AG9B65PV6B PLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG (ACETAMINOPHEN) TABLET [PROFICIENT RX LP] 1 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ ACETAMINOPHEN TABLET [REBEL DISTRIBUTORS CORP] 1 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ PLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG (ACETAMINOPHEN) TABLET [PROFICIENT RX LP] 1 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP PLUSPHARMA EXTRA STRENGTH PAIN RELIEVER,FEVER REDUCER 500 MG (ACETAMINOPHEN) TABLET [PROFICIENT RX LP] 1 STEARIC ACID INACTIVE INGREDIENT 4ELV7Z65AP ACETAMINOPHEN TABLET [REBEL DISTRIBUTORS CORP] 1
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 51645-706-01 51645070601 100 TABLET in 1 BOTTLE, PLASTIC (51645-706-01) 100 tablet 2006-03-27 0000-00-00 No No Current 51645-706-10 51645070610 1000 TABLET in 1 BOTTLE, PLASTIC (51645-706-10) 1000 tablet 2006-03-27 0000-00-00 No No Current