FDA.reportPublic FDA data

Sunmark Aspirin

Product NDC
49348-001
Requested package NDC
49348-001-14
11-digit product format
493480001
Labeler code
49348
Product ID
49348-001_3faeeedb-6301-424b-a4fb-bec334c2f4ac
Type
HUMAN OTC DRUG
Nonproprietary name
Aspirin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Strategic Sourcing Services LLC
Application
part343
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2003-06-24
Marketing end
0000-00-00
Substance
ASPIRIN
Active strength
325 mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
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 packagepackage49348-00149348-001-14DDiscontinued by firm2026-09-14

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 dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…
2024-11-09 02:27 UTC · source 2024-11-08ad56d346431e…cc804d4bbf1e…
2024-10-04 04:10 UTC · source 2024-10-03367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09557ba5c1ecfa…9c80585c8c6e…

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49348-001-10EA - Each49348-0014d34bde8-1c89-4023-b78f-87052e2f58b712012-07-24
49348-001-14EA - Each49348-001a311838d-d235-4f26-a334-8ae49432114a12012-07-24
49348-001-23EA - Each49348-00134cd5d1d-f69d-478e-b4aa-5084a93ab52712012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ASPIRINACTIVE INGREDIENTR16CO5Y76ESUNMARK ASPIRIN REGULAR STRENGTH (ASPIRIN) TABLET [MCKESSON]2
ASPIRINACTIVE MOIETYR16CO5Y76ESUNMARK ASPIRIN REGULAR STRENGTH (ASPIRIN) TABLET [MCKESSON]2
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATEINACTIVE INGREDIENTO7TSZ97GEPSUNMARK ASPIRIN REGULAR STRENGTH (ASPIRIN) TABLET [MCKESSON]2
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOSUNMARK ASPIRIN REGULAR STRENGTH (ASPIRIN) TABLET [MCKESSON]2
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJSUNMARK ASPIRIN REGULAR STRENGTH (ASPIRIN) TABLET [MCKESSON]2
TALCINACTIVE INGREDIENT7SEV7J4R1USUNMARK ASPIRIN REGULAR STRENGTH (ASPIRIN) TABLET [MCKESSON]2
TRIACETININACTIVE INGREDIENTXHX3C3X673SUNMARK ASPIRIN REGULAR STRENGTH (ASPIRIN) TABLET [MCKESSON]2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
49348-001-1449348000114500 TABLET, FILM COATED in 1 BOTTLE (49348-001-14) 2003-08-210000-00-00NoNoCurrent