Home NDC 55289-880 Acetaminophen
Product NDC 55289-880
11-digit product format 552890880
Labeler code 55289
Product ID 55289-880_48390181-cda8-a543-e063-6294a90a5896
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET
Route ORAL
Labeler PD-Rx Pharmaceuticals, Inc.
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2006-01-10
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 2027-12-31 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 55289-880-01 Acetaminophen 100 in 1 BOTTLE, PLASTIC TABLET 100 17 55289-880-06 Acetaminophen 6 in 1 BOTTLE, PLASTIC TABLET 6 17 55289-880-12 Acetaminophen 12 in 1 BOTTLE, PLASTIC TABLET 12 17 55289-880-20 Acetaminophen 20 in 1 BOTTLE, PLASTIC TABLET 20 17 55289-880-21 Acetaminophen 21 in 1 BOTTLE, PLASTIC TABLET 21 17 55289-880-24 Acetaminophen 24 in 1 BOTTLE, PLASTIC TABLET 24 17 55289-880-30 Acetaminophen 30 in 1 BOTTLE, PLASTIC TABLET 30 17 55289-880-50 Acetaminophen 50 in 1 BOTTLE, PLASTIC TABLET 50 17 55289-880-60 Acetaminophen 60 in 1 BOTTLE, PLASTIC TABLET 60 17 55289-880-97 Acetaminophen 200 in 1 BOTTLE, PLASTIC TABLET 200 17
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55289-880 ACETAMINOPHEN TABLET [PD-RX PHARMACEUTICALS, INC.] 14 Current NDC, Legacy NDC, 10 package rows 20250322_64696f65-415e-4ce1-a5b3-70662fbcb002.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 64 of 79 · 1,570 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Pain and Fever ACETAMINOPHEN H E B 86a072a9-c3b8-47f7-8598-d66e3d30e762 2024-08-21 Warnings Exact identifier application number: M013 Childrens Pain and Fever ACETAMINOPHEN Kroger Company d965eba0-b268-41b2-8e02-5f6d769a44d7 2024-08-18 Warnings Exact identifier application number: M013 equate pain and fever childrens ACETAMINOPHEN Wal-Mart Stores Inc ea68d735-c677-4280-a3a3-ae3eb5ff7462 2024-08-17 Warnings Exact identifier application number: M013 childrens pain and fever ACETAMINOPHEN CVS Pharmacy fac408f0-ebb6-4c72-88ee-2ba85867859c 2024-08-16 Warnings Exact identifier application number: M013 Regular Strength Pain Relief ACETAMINOPHEN Bryant Ranch Prepack 3f0c32b1-2c54-4ca3-9759-9e5dd9d7ad24 2024-08-14 Warnings Exact identifier application number: M013 Quality Choice Effervescent Antacid and Pain Relief - Extra Strength ASPIRIN, ANHYDROUS CITRIC ACID, SODIUM BICARBONATE Chain Drug Marketing Association 1f926637-a61c-8eb7-e063-6394a90a6502 2024-08-13 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN PAI Holdings, LLC dba PAI Pharma 6ec12573-03d6-40c1-9945-d345b401e062 2024-08-12 Warnings Exact identifier application number: M013 CareOne Infants Acetaminophen ACETAMINOPHEN American Sales Company eacee273-abd7-4ea4-bcaa-7f74abcc9feb 2024-08-07 Warnings Exact identifier application number: M013 infants pain and fever ACETAMINOPHEN Kroger Company 7dbe284a-c0d5-4ac4-8445-611610f3c0fb 2024-08-02 Warnings Exact identifier application number: M013 Dollar General Effervescent Pain Reliever ASPIRIN Dolgencorp, Inc 1deab362-a325-3a00-e063-6294a90a9acd 2024-08-01 Warnings Exact identifier application number: M013 Acetaminophen Extra Strength ACETAMINOPHEN FSA STORE INC. 1cd6a3e6-1376-0b7b-e063-6394a90af3d1 2024-07-30 Warnings Exact identifier application number: M013 pain relief pm extra strength ACETAMINOPHEN, DIPHENHYDRAMINE HCL Publix Super Markets Inc 42d271b7-b45f-4497-8de2-4e05b4bebfa9 2024-07-17 Warnings Exact identifier application number: M013 basic care acetaminophen pm ACETAMINOPHEN, DIPHENHYDRAMINE HCL Amazon.com Services LLC 64a0084a-e29e-4c1a-8704-13a3e1238f76 2024-07-17 Warnings Exact identifier application number: M013 Low Dose Aspirin ASPIRIN Walmart Inc. 152c013a-c81c-f8f9-e063-6294a90a9f23 2024-07-15 Warnings Exact identifier application number: M013 Diphenhydramine HCL DIPHENHYDRAMINE HCL NuCare Pharmaceuticals, Inc. 5411544e-3c2d-4e42-e054-00144ff8d46c 2024-07-10 Warnings Exact identifier application number: M013 good sense pain relief pm extra strength ACETAMINOPHEN, DIPHENHYDRAMINE HCL L. Perrigo Company b97c51ad-4953-4491-9ceb-395550eb5296 2024-07-10 Warnings Exact identifier application number: M013 Headache Relief Extra Strength ACETAMINOPHEN, ASPIRIN, CAFFEINE Walgreens 065e6f1b-f68c-491a-a157-84961a07e3d9 2024-07-10 Warnings Exact identifier application number: M013 Headache Relief Extra Strength ACETAMINOPHEN, ASPIRIN, CAFFEINE Walgreens 3b7b6725-2996-44d3-89a3-032384e7e2ce 2024-07-10 Warnings Exact identifier application number: M013 equate pain and fever infants ACETAMINOPHEN Wal-Mart Stores Inc 8a152c8d-8ae0-4201-8bb9-7b22c3577415 2024-07-10 Warnings Exact identifier application number: M013 Acetaminophen PM Extra Strength ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE WinCo Foods, LLC 3c57498c-86b0-4ba3-881e-c742a2e8ece5 2024-07-09 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 55289-880-01 55289088001 100 TABLET in 1 BOTTLE, PLASTIC (55289-880-01) 100 tablet 2018-01-12 0000-00-00 No No Current 55289-880-06 55289088006 6 TABLET in 1 BOTTLE, PLASTIC (55289-880-06) 6 tablet 2021-03-26 0000-00-00 No No Current 55289-880-12 55289088012 12 TABLET in 1 BOTTLE, PLASTIC (55289-880-12) 12 tablet 2021-03-26 0000-00-00 No No Current 55289-880-20 55289088020 20 TABLET in 1 BOTTLE, PLASTIC (55289-880-20) 20 tablet 2019-09-09 0000-00-00 No No Current 55289-880-21 55289088021 21 TABLET in 1 BOTTLE, PLASTIC (55289-880-21) 21 tablet 2025-12-16 No No Current 55289-880-24 55289088024 24 TABLET in 1 BOTTLE, PLASTIC (55289-880-24) 24 tablet 2025-05-29 0000-00-00 No No Current 55289-880-30 55289088030 30 TABLET in 1 BOTTLE, PLASTIC (55289-880-30) 30 tablet 2018-01-12 0000-00-00 No No Current 55289-880-50 55289088050 50 TABLET in 1 BOTTLE, PLASTIC (55289-880-50) 50 tablet 2021-03-26 0000-00-00 No No Current 55289-880-60 55289088060 60 TABLET in 1 BOTTLE, PLASTIC (55289-880-60) 60 tablet 2021-03-26 0000-00-00 No No Current 55289-880-97 55289088097 200 TABLET in 1 BOTTLE, PLASTIC (55289-880-97) 200 tablet 2021-03-26 0000-00-00 No No Current