Home NDC 71205-517-90 Tri-Buffered Aspirin
Product NDC 71205-517
Requested package NDC 71205-517-90
11-digit product format 712050517
Labeler code 71205
Product ID 71205-517_ccda47aa-2aeb-4e29-b140-bb903d516bbf
Type HUMAN OTC DRUG
Nonproprietary name Aspirin
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Proficient Rx LP
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 1990-03-30
Substance ASPIRIN
Active strength 325 mg/1
Pharmacologic classes Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation Inhibitor [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Tri-Buffered Aspirin
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ASPIRIN 325 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination R16CO5Y76E Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 212033 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71205-517-30 Tri-Buffered Aspirin 30 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 30 4 71205-517-60 Tri-Buffered Aspirin 60 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 60 4 71205-517-90 Tri-Buffered Aspirin 90 in 1 BOTTLE, PLASTIC TABLET, FILM COATED 90 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71205-517 TRI-BUFFERED ASPIRIN (ASPIRIN) TABLET, FILM COATED [PROFICIENT RX LP] 4 Current NDC, Legacy NDC, 3 package rows 20231013_640c3311-2abf-40b2-82b9-9fe4d8c1cf1d.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 84 · 1,678 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 71205-517-90 71205051790 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-517-90) 2020-12-30 0000-00-00 No No Current