Home NDC 69848-003-24 Acetaminophen
Product NDC 69848-003
Requested package NDC 69848-003-24
11-digit product format 698480003
Labeler code 69848
Product ID 69848-003_468e5f4e-8bc6-6b97-e063-6294a90a0166
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET
Route ORAL
Labeler Granules USA, Inc
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-07-01
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 · 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 2020-12-18 03:04 UTC · source 2020-12-17 excluded package package 69848-003 69848-003-24 I Inactivated by FDA excluded / ndc_excluded.zip e2bbac7714bc…27bdfed8d636…
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 Acetaminophen
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.
FDA-Initiated Inactive NDC Indexing# NDC, Effective, Related label table NDC Effective Related label 69848-003-10 2020-12-30 EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS 69848-003-17 2020-12-30 EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS 69848-003-24 2020-12-30 EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS 69848-003-10 2020-09-27 EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS 69848-003-17 2020-09-27 EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS 69848-003-24 2020-09-27 EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS 69848-003-10 2020-09-25 EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS 69848-003-17 2020-09-25 EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS 69848-003-24 2020-09-25 EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS 69848-003-10 2020-07-22 EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS 69848-003-17 2020-07-22 EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS 69848-003-24 2020-07-22 EXTRA STRENGTH Pain Relief Acetaminophen USP,500 mg Pain Reliever/Fever Reducer FOR ADULTS
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69848-003-10 Acetaminophen 100 in 1 BOTTLE TABLET 100 8 69848-003-17 Acetaminophen 175 in 1 BOTTLE TABLET 175 8 69848-003-24 Acetaminophen 24 in 1 BOTTLE TABLET 24 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69848-003 ACETAMINOPHEN TABLET [GRANULES USA, INC] 7 Current NDC, Legacy NDC, 3 package rows 20241218_a1255f60-b9c6-9a95-e053-2995a90a9e80.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 60 of 79 · 1,561 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join LOW DOSE ASPIRIN ASPIRIN DISCOUNT DRUG MART af0f50d2-3e2d-f723-e053-2995a90a0d4b 2024-10-16 Warnings Exact identifier application number: M013 Enteric Coated Aspirin ASPIRIN DISCOUNT DRUG MART 03ed19dd-1cfc-47d5-b83e-ffa2ebe93f48 2024-10-16 Warnings Exact identifier application number: M013 PAIN RELIEF Regular Strength ACETAMINOPHEN AMERICAN SALES COMPANY 2e3eabc8-193b-4397-a43c-db838eb16e67 2024-10-15 Warnings Exact identifier application number: M013 Chewable Aspirin ASPIRIN RETAIL BUSINESS SERVICES , LLC. c94d68ea-7f25-881f-e053-2995a90aa47f 2024-10-15 Warnings Exact identifier application number: M013 LOW DOSE ASPIRIN ASPIRIN RETAIL BUSINESS SERVICES , LLC. c94d750e-5a85-77f5-e053-2995a90a6915 2024-10-15 Warnings Exact identifier application number: M013 Infants Pain and Fever ACETAMINOPHEN Walgreen Company 9e08eb38-7538-4fa0-a0e1-047ab6cb1680 2024-10-15 Warnings Exact identifier application number: M013 pain relief ACETAMINOPHEN PUBLIX SUPER MARKETS INC 9e779cc6-4641-6132-e053-2a95a90a3493 2024-10-11 Warnings Exact identifier application number: M013 Pain Reliever ACETAMINOPHEN CHAIN DRUG CONSORTIUM 5c1a3081-ae25-4895-bf76-ebcbb9fc8072 2024-10-11 Warnings Exact identifier application number: M013 Aspirin 81 MG ASPIRIN Meijer b3e5711c-9529-4eec-871d-de8efa858b86 2024-10-11 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN MEIJER DISTRIBUTION INC 9586e830-a285-4a07-8b34-969875442348 2024-10-11 Warnings Exact identifier application number: M013 Pain Relief Extra Strength ACETAMINOPHEN Chain Drug Marketing Association 68a52858-35c5-402a-8ceb-8d8a7c1e5f6c 2024-10-11 Warnings Exact identifier application number: M013 Pain Relief Extra Strength ACETAMINOPHEN Chain Drug Marketing Association 5de40821-3218-4320-bf11-9493bf01d489 2024-10-11 Warnings Exact identifier application number: M013 Pain Relief PM Extra Strength ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE Chain Drug Marketing Association 475becec-1a56-4cfa-a0c5-562f8772adfb 2024-10-11 Warnings Exact identifier application number: M013 Topcare Pain Relief ACETAMINOPHEN Topco Associates LLC 6036c15b-1168-4103-9471-6a74a2140e53 2024-10-10 Warnings Exact identifier application number: M013 Childrens Acetaminophen ACETAMINOPHEN PAI Holdings, LLC dba PAI Pharma 46d9d8cd-e3db-492c-9386-7e8255beff64 2024-10-08 Warnings Exact identifier application number: M013 dg health aspirin ASPIRIN Dolgencorp, LLC 0ab34dc7-0110-4fc3-ae53-234e7d7bca3c 2024-10-07 Warnings Exact identifier application number: M013 ValuMeds Pain Relief PM Pain Reliever and Nighttime Sleep Aid Acetaminophen, Extra Strength ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE Cabinet Health P.B.C. 19ba1fb6-22ea-488e-9e52-94c14ceb80d1 2024-10-07 Warnings Exact identifier application number: M013 foster and thrive aspirin ASPIRIN Strategic Sourcing Services LLC 4d66a8a8-a1c1-4430-8845-21ae67700c39 2024-10-07 Warnings Exact identifier application number: M013 leader aspirin ASPIRIN Cardinal Health 110, LLC. dba Leader ca603b12-e0f7-4d79-8e0d-4651a788ba9b 2024-10-07 Warnings Exact identifier application number: M013 foster and thrive aspirin ASPIRIN McKesson Medical-Surgical, Inc. e9342478-93d6-45de-948f-f4162ee675b2 2024-10-07 Warnings Exact identifier application number: M013
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 69848-003-24 69848000324 24 TABLET in 1 BOTTLE (69848-003-24) 24 tablet 2019-07-01 0000-00-00 No No Current