Home NDC 0904-7481 Acetaminophen
Product NDC 0904-7481
11-digit product format 009047481
Labeler code 0904
Product ID 0904-7481_072e6688-f9f2-409b-8b89-c558e785ba16
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form SOLUTION
Route ORAL
Labeler Major Pharmaceuticals
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-07-15
Substance ACETAMINOPHEN
Active strength 1000 mg/30mL
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 1000 mg/30mL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0904-7481-59 Acetaminophen 237 mL in 1 BOTTLE, PLASTIC SOLUTION 237 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0904-7481 ACETAMINOPHEN SOLUTION [MAJOR PHARMACEUTICALS] 1 Current NDC, 1 package rows 20241009_e1a55e0d-bb86-4515-8436-51a74b403685.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 78 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 Sample Exclude flag Status 0904-7481-59 00904748159 237 mL in 1 BOTTLE, PLASTIC (0904-7481-59) 237 ml 2021-07-15 No No Current