Home NDC 69729-800 ATAMEL Forte
Product NDC 69729-800
11-digit product format 697290800
Labeler code 69729
Product ID 69729-800_5ca4c11a-688b-3d5d-e063-6394a90ae677
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, COATED
Route ORAL
Labeler OPMX LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-01-29
Substance ACETAMINOPHEN
Active strength 650 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 ATAMEL Forte
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 650 mg/1
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69729-800-24 ATAMEL Forte 12 in 1 BLISTER PACK TABLET, COATED 12 1 69729-800-24 ATAMEL Forte 2 in 1 CARTON TABLET, COATED 2 1
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 2 of 83 · 1,657 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 69729-800-24 69729080024 2 BLISTER PACK in 1 CARTON (69729-800-24) / 12 TABLET, COATED in 1 BLISTER PACK 2 blister pack 2026-01-29 No No Current