Home NDC 49035-914-32 Aspirin
Product NDC 49035-914
Requested package NDC 49035-914-32
11-digit product format 490350914
Labeler code 49035
Product ID 49035-914_70f66f99-a450-4ab6-a3b9-c5d9207e0a79
Type HUMAN OTC DRUG
Nonproprietary name Aspirin
Dosage form TABLET, DELAYED RELEASE
Route ORAL
Labeler Wal-Mart Stores Inc
Application part343
Marketing category OTC MONOGRAPH NOT FINAL
Marketing start 2014-07-25
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 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 · 12 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…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ASPIRIN ACTIVE INGREDIENT R16CO5Y76E ASPIRIN ADULT LOW DOSE (ASPIRIN) TABLET, COATED [WAL-MART STORES INC] 2 ASPIRIN ACTIVE MOIETY R16CO5Y76E ASPIRIN ADULT LOW DOSE (ASPIRIN) TABLET, COATED [WAL-MART STORES INC] 2 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U ASPIRIN ADULT LOW DOSE (ASPIRIN) TABLET, COATED [WAL-MART STORES INC] 2 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA ASPIRIN ADULT LOW DOSE (ASPIRIN) TABLET, COATED [WAL-MART STORES INC] 2 FD&C YELLOW NO. 6 INACTIVE INGREDIENT H77VEI93A8 ASPIRIN ADULT LOW DOSE (ASPIRIN) TABLET, COATED [WAL-MART STORES INC] 2 HYPROMELLOSES INACTIVE INGREDIENT 3NXW29V3WO ASPIRIN ADULT LOW DOSE (ASPIRIN) TABLET, COATED [WAL-MART STORES INC] 2 METHACRYLIC ACID INACTIVE INGREDIENT 1CS02G8656 ASPIRIN ADULT LOW DOSE (ASPIRIN) TABLET, COATED [WAL-MART STORES INC] 2 POLYDEXTROSE INACTIVE INGREDIENT VH2XOU12IE ASPIRIN ADULT LOW DOSE (ASPIRIN) TABLET, COATED [WAL-MART STORES INC] 2 POLYETHYLENE GLYCOLS INACTIVE INGREDIENT 3WJQ0SDW1A ASPIRIN ADULT LOW DOSE (ASPIRIN) TABLET, COATED [WAL-MART STORES INC] 2 SHELLAC INACTIVE INGREDIENT 46N107B71O ASPIRIN ADULT LOW DOSE (ASPIRIN) TABLET, COATED [WAL-MART STORES INC] 2 SODIUM BICARBONATE INACTIVE INGREDIENT 8MDF5V39QO ASPIRIN ADULT LOW DOSE (ASPIRIN) TABLET, COATED [WAL-MART STORES INC] 2 SODIUM LAURYL SULFATE INACTIVE INGREDIENT 368GB5141J ASPIRIN ADULT LOW DOSE (ASPIRIN) TABLET, COATED [WAL-MART STORES INC] 2 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ ASPIRIN ADULT LOW DOSE (ASPIRIN) TABLET, COATED [WAL-MART STORES INC] 2 TALC INACTIVE INGREDIENT 7SEV7J4R1U ASPIRIN ADULT LOW DOSE (ASPIRIN) TABLET, COATED [WAL-MART STORES INC] 2 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP ASPIRIN ADULT LOW DOSE (ASPIRIN) TABLET, COATED [WAL-MART STORES INC] 2 TRIACETIN INACTIVE INGREDIENT XHX3C3X673 ASPIRIN ADULT LOW DOSE (ASPIRIN) TABLET, COATED [WAL-MART STORES INC] 2 TRIETHYL CITRATE INACTIVE INGREDIENT 8Z96QXD6UM ASPIRIN ADULT LOW DOSE (ASPIRIN) TABLET, COATED [WAL-MART STORES INC] 2
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 49035-914-32 49035091432 1 BOTTLE, PLASTIC in 1 CARTON (49035-914-32) > 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC 2014-07-25 0000-00-00 No No Current