Home NDC 49035-563-96 Low Dose Aspirin
Product NDC 49035-563
Requested package NDC 49035-563-96
11-digit product format 490350563
Labeler code 49035
Product ID 49035-563_ea158083-c7a0-4b01-aa1d-d0e41bdc5e70
Type HUMAN OTC DRUG
Nonproprietary name Aspirin
Dosage form TABLET, DELAYED RELEASE
Route ORAL
Labeler Wal-Mart Stores Inc
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-05-01
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 2027-12-31
Current FDA listing Yes 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 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…
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 Low Dose Aspirin
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ASPIRIN 81 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 308416 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 49035-563-11 Low Dose Aspirin 60 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 60 20 49035-563-11 Low Dose Aspirin 1 in 1 CARTON TABLET, DELAYED RELEASE 1 20 49035-563-13 Low Dose Aspirin 250 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 250 20 49035-563-13 Low Dose Aspirin 2 in 1 CARTON TABLET, DELAYED RELEASE 2 20 49035-563-14 Low Dose Aspirin 500 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 500 20 49035-563-17 Low Dose Aspirin 300 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 300 20 49035-563-27 Low Dose Aspirin 32 in 1 BOTTLE TABLET, DELAYED RELEASE 32 20 49035-563-27 Low Dose Aspirin 1 in 1 CARTON TABLET, DELAYED RELEASE 1 20 49035-563-32 Low Dose Aspirin 1 in 1 CARTON TABLET, DELAYED RELEASE 1 20 49035-563-32 Low Dose Aspirin 120 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 120 20 49035-563-96 Low Dose Aspirin 250 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 250 20 49035-563-96 Low Dose Aspirin 2 in 1 CARTON TABLET, DELAYED RELEASE 2 20
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49035-563 LOW DOSE ASPIRIN (ASPIRIN) TABLET, DELAYED RELEASE [WAL-MART STORES INC] 19 Current NDC, Legacy NDC, 12 package rows 20250519_093e0458-9975-456f-8950-8273c8890b3c.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 83 · 1,657 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 49035-563-96 49035056396 2 BOTTLE, PLASTIC in 1 CARTON (49035-563-96) > 250 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2011-05-01 0000-00-00 No No Current