Aspirin 81 mg

Product NDC
71406-128
Requested package NDC
71406-128-10
11-digit product format
714060128
Labeler code
71406
Product ID
71406-128_eb8f03f8-0f11-7524-e053-2a95a90a3bfe
Type
HUMAN OTC DRUG
Nonproprietary name
Aspirin Enteric Coated Tablets 81 mg
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
AACE Pharmaceuticals, Inc.
Application
part343
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-05-03
Marketing end
0000-00-00
Substance
ASPIRIN
Active strength
81 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
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage71406-12871406-128-10DDiscontinued by firm2026-10-12

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage71406-12871406-128-10DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage71406-12871406-128-10DDiscontinued by firmexcluded / ndc_excluded.zipf5e01cc5f278…a2eaf40c39c3…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71406-128-10EA - Each71406-128ba1e361e-bbbe-4e71-aa9a-1982b0ae106612021-11-09
71406-128-12EA - Each71406-128d026f40a-0608-4bb3-b1e6-d53c51eb850612021-11-09

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71406-128-10714060128101000 TABLET, DELAYED RELEASE in 1 BOTTLE (71406-128-10) 2021-05-140000-00-00NoNoCurrent