FDA.reportPublic FDA data

Mapap

Product NDC
49999-131
Requested package NDC
49999-131-30
11-digit product format
499990131
Labeler code
49999
Product ID
49999-131_ba43904f-a40f-4bcf-9a75-2065f912fda6
Type
HUMAN OTC DRUG
Nonproprietary name
ACETAMINOPHEN
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
part343
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2011-04-21
Marketing end
0000-00-00
Substance
ACETAMINOPHEN
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 packagepackage49999-13149999-131-30DDiscontinued by firm2026-10-05

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…

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
49999-131-30EA - Each49999-131270ca21f-54cc-4cbd-b2cc-b2c3dd0e09d612013-09-04

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACETAMINOPHENACTIVE INGREDIENT362O9ITL9DMAPAP (ACETAMINOPHEN) TABLET [LAKE ERIE MEDICAL DBA QUALITY CARE PRODUCTS LLC]1
ACETAMINOPHENACTIVE MOIETY362O9ITL9DMAPAP (ACETAMINOPHEN) TABLET [LAKE ERIE MEDICAL DBA QUALITY CARE PRODUCTS LLC]1
POVIDONEINACTIVE INGREDIENTFZ989GH94EMAPAP (ACETAMINOPHEN) TABLET [LAKE ERIE MEDICAL DBA QUALITY CARE PRODUCTS LLC]1
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A2MAPAP (ACETAMINOPHEN) TABLET [LAKE ERIE MEDICAL DBA QUALITY CARE PRODUCTS LLC]1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJMAPAP (ACETAMINOPHEN) TABLET [LAKE ERIE MEDICAL DBA QUALITY CARE PRODUCTS LLC]1
STEARIC ACIDINACTIVE INGREDIENT4ELV7Z65APMAPAP (ACETAMINOPHEN) TABLET [LAKE ERIE MEDICAL DBA QUALITY CARE PRODUCTS LLC]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
49999-131-304999901313030 TABLET in 1 BOTTLE, PLASTIC (49999-131-30) 30 tablet2011-04-210000-00-00NoNoCurrent