Home NDC 49035-919 Pain Reliever
Product NDC 49035-919
11-digit product format 490350919
Labeler code 49035
Product ID 49035-919_d9aaffe0-1e65-4716-93b9-c344370e2c07
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, COATED
Route ORAL
Labeler Wal-Mart Stores Inc
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-11-26
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 Pain Reliever
Brand name suffix Extra Strength
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 49035-919-08 Pain RelieverExtra Strength 1 in 1 CARTON TABLET, COATED 1 8 49035-919-08 Pain RelieverExtra Strength 24 in 1 BOTTLE, PLASTIC TABLET, COATED 24 8 49035-919-12 Pain RelieverExtra Strength 100 in 1 BOTTLE, PLASTIC TABLET, COATED 100 8 49035-919-20 Pain RelieverExtra Strength 225 in 1 BOTTLE, PLASTIC TABLET, COATED 225 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49035-919 PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) TABLET, COATED [WAL-MART STORES INC] 6 Current NDC, Legacy NDC, 4 package rows 20241027_72365264-f9c4-49f0-be64-73d95817d358.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 1 of 83 · 1,657 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 49035-919-08 49035091908 1 BOTTLE, PLASTIC in 1 CARTON (49035-919-08) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC 2019-11-26 0000-00-00 No No Current 49035-919-12 49035091912 100 TABLET, COATED in 1 BOTTLE, PLASTIC (49035-919-12) 2019-11-26 0000-00-00 No No Current 49035-919-20 49035091920 225 TABLET, COATED in 1 BOTTLE, PLASTIC (49035-919-20) 2019-11-26 0000-00-00 No No Current