Aspirin

Product NDC
49638-102
Requested package NDC
49638-102-60
11-digit product format
496380102
Labeler code
49638
Product ID
49638-102_c7429a4f-4710-2c68-e053-2a95a90ab3a0
Type
HUMAN OTC DRUG
Nonproprietary name
Aspirin
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Labeler
America Medic & Science, LLC
Application
part343
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-06-29
Marketing end
0000-00-00
Substance
ASPIRIN
Active strength
81 mg/1
NDC exclude flag
No
Listing certified through
2022-12-31
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 packagepackage49638-10249638-102-60DDiscontinued by firm2026-10-05

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49638-102ASPIRIN TABLET, DELAYED RELEASE [AMERICA MEDIC & SCIENCE, LLC]8Legacy NDC20240206_88cb580d-64ec-4762-be76-71cccdc07f18.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49638-102-60496380102601 BOTTLE in 1 CARTON (49638-102-60) > 60 TABLET, DELAYED RELEASE in 1 BOTTLE1 bottle2021-06-290000-00-00NoNoCurrent