Home NDC 82706-007 NOTTS - Extra Strength 500 mg
Product NDC 82706-007
11-digit product format 827060007
Labeler code 82706
Product ID 82706-007_2df54d96-b18b-e9e3-e063-6294a90a6926
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET
Route ORAL
Labeler VIVUNT PHARMA LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-08-17
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 · 3 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 2024-11-09 02:27 UTC · source 2024-11-08 excluded package package 82706-007 82706-007-04 D Discontinued by firm excluded / ndc_excluded.zip ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 excluded package package 82706-007 82706-007-04 D Discontinued by firm excluded / ndc_excluded.zip 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 82706-007 82706-007-04 D Discontinued by firm excluded / ndc_excluded.zip 557ba5c1ecfa…9c80585c8c6e…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base NOTTS - Extra Strength 500 mg
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 500 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198440 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 82706-007-01 NOTTS - Extra Strength 500 mg 1 in 1 CARTON TABLET 1 12 82706-007-01 NOTTS - Extra Strength 500 mg 24 in 1 BOTTLE, PLASTIC TABLET 24 12 82706-007-02 NOTTS - Extra Strength 500 mg 100 in 1 BOTTLE, PLASTIC TABLET 100 12 82706-007-02 NOTTS - Extra Strength 500 mg 1 in 1 CARTON TABLET 1 12 82706-007-03 NOTTS - Extra Strength 500 mg 400 in 1 BOTTLE, PLASTIC TABLET 400 12 82706-007-04 NOTTS - Extra Strength 500 mg 2 in 1 POUCH TABLET 2 12 82706-007-04 NOTTS - Extra Strength 500 mg 3 in 1 CARTON TABLET 3 12 82706-007-05 NOTTS - Extra Strength 500 mg 2 in 1 POUCH TABLET 2 12 82706-007-05 NOTTS - Extra Strength 500 mg 50 in 1 CARTON TABLET 50 12 82706-007-06 NOTTS - Extra Strength 500 mg 25 in 1 CARTON TABLET 25 12 82706-007-06 NOTTS - Extra Strength 500 mg 25 in 1 BLISTER PACK TABLET 25 12
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82706-007 NOTTS - EXTRA STRENGTH 500 MG (ACETAMINOPHEN) TABLET [VIVUNT PHARMA LLC] 12 Current NDC, Legacy NDC, 11 package rows 20250215_e677f43d-b4ce-e5b0-e053-2a95a90ad67e.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 39 of 79 · 1,579 matching rows.
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 82706-007-01 82706000701 1 BOTTLE, PLASTIC in 1 CARTON (82706-007-01) / 24 TABLET in 1 BOTTLE, PLASTIC 2022-08-17 0000-00-00 No No Current 82706-007-02 82706000702 1 BOTTLE, PLASTIC in 1 CARTON (82706-007-02) / 100 TABLET in 1 BOTTLE, PLASTIC 2022-08-17 0000-00-00 No No Current 82706-007-03 82706000703 400 TABLET in 1 BOTTLE, PLASTIC (82706-007-03) 400 tablet 2022-08-17 0000-00-00 No No Current 82706-007-04 82706000704 3 POUCH in 1 CARTON (82706-007-04) / 2 TABLET in 1 POUCH 3 pouch 2023-09-20 No No Current 82706-007-05 82706000705 50 POUCH in 1 CARTON (82706-007-05) / 2 TABLET in 1 POUCH 50 pouch 2024-07-05 No No Current 82706-007-06 82706000706 25 BLISTER PACK in 1 CARTON (82706-007-06) / 25 TABLET in 1 BLISTER PACK 25 blister pack 2025-02-12 No No Current