Home NDC 68071-3425 Aspirin
Product NDC 68071-3425
11-digit product format 680713425
Labeler code 68071
Product ID 68071-3425_5a869477-29e0-2b45-e063-6294a90adcf6
Type HUMAN OTC DRUG
Nonproprietary name Aspirin
Dosage form TABLET, DELAYED RELEASE
Route ORAL
Labeler NuCare Pharmaceuticals,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 · 18 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 68071-3425-9 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 excluded product product I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-08-27 00:01 UTC · source 2025-08-26 excluded package package 68071-3425-9 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 excluded product product I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-04-01 02:39 UTC · source 2025-03-31 excluded package package 68071-3425-9 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 excluded product product I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-28 20:22 UTC · source 2025-03-28 excluded package package 68071-3425-9 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 excluded product product I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-22 03:12 UTC · source 2025-03-21 excluded package package 68071-3425-9 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 excluded product product I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 68071-3425-9 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 excluded product product U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-02-02 03:52 UTC · source 2025-01-31 excluded package package 68071-3425-9 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 excluded product product U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-20 13:05 UTC · source 2025-01-20 excluded package package 68071-3425-9 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 excluded product product U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 68071-3425-9 U Excluded because listing certification expired 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 Aspirin
Brand name suffix Low Dose
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ASPIRIN 81 mg/1
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68071-3425-9 AspirinLow Dose 90 in 1 BOTTLE, PLASTIC TABLET, DELAYED RELEASE 90 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68071-3425 ASPIRIN LOW DOSE (ASPIRIN) TABLET, DELAYED RELEASE [NUCARE PHARMACEUTICALS,INC.] 3 Current NDC, 1 package rows 20230629_fd199a7f-76ca-fefc-e053-6294a90a821d.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 75 of 79 · 1,576 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Alka-Seltzer BUFFERED ASPIRIN Lil' Drug Store Products, Inc. 0c7a60e7-0bde-9aa2-e063-6294a90a3209 2023-12-14 Warnings Exact identifier application number: M013 Circle K Aspirin 325 ASPIRIN Lil Drug Store Products, Inc 4cd306e3-2119-4272-9da4-a848fe2746fa 2023-12-14 Warnings Exact identifier application number: M013 Circle K Pain Reliever Extra Strength ACETAMINOPHEN Lil' Drug Store Products, Inc. f2359bc3-901f-4ecb-b402-cb2fe404a935 2023-12-14 Warnings Exact identifier application number: M013 Childrens Pain Relief ACETAMINOPHEN DISCOUNT DRUG MART c55b8f9d-1396-43c0-acc9-5e3485eadb07 2023-12-08 Warnings Exact identifier application number: M013 Childrens Pain Relief ACETAMINOPHEN DISCOUNT DRUG MART 775519ad-5683-451f-9bfc-5fafc70c68ec 2023-12-08 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN WALGREEN CO. c20c814b-35f5-4c46-e053-2a95a90a50f2 2023-12-08 Warnings Exact identifier application number: M013 Acetaminophen Extra Strength ACETAMINOPHEN Better Living Brands LLC f9859be4-6d0b-2ab8-e053-6294a90aa862 2023-12-06 Warnings Exact identifier application number: M013 Aurophen Regular Strength ACETAMINOPHEN KROGER COMPANY b9b7b849-c3b3-9af7-e053-2a95a90a0077 2023-12-06 Warnings Exact identifier application number: M013 Acetaminophen Regular Strength ACETAMINOPHEN KROGER COMPANY cf649478-57d2-cc88-e053-2a95a90ad1ba 2023-12-06 Warnings Exact identifier application number: M013 Acetaminophen Extra Strength ACETAMINOPHEN KROGER COMPANY b9b6f878-1ec8-3dc0-e053-2995a90a5414 2023-12-06 Warnings Exact identifier application number: M013 Pain Reliever ACETAMINOPHEN WALGREEN CO. a48c522c-76c5-49f8-8c4d-3ee6b221e6f3 2023-12-06 Warnings Exact identifier application number: M013 Pain Reliever ACETAMINOPHEN WALGREEN CO. cc939a7c-ce56-5dd6-e053-2995a90aa8af 2023-12-06 Warnings Exact identifier application number: M013 Alka-Seltzer Original Flavor BUFFERED ASPIRIN, EFFERVESCENT TABLET Lil' Drug Store Products, Inc. ea5df8be-a08c-5fa3-e053-2995a90a0bac 2023-12-06 Warnings Exact identifier application number: M013 Ringl ACETAMINOPHEN Sato Pharmaceutical Co., Ltd. ba5a0286-3e0f-4bef-96e5-29d92f51f432 2023-12-06 Warnings Exact identifier application number: M013 Pain Relief Childrens ACETAMINOPHEN Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) 41633554-474e-4d3c-9187-d90487d2ae8c 2023-12-06 Warnings Exact identifier application number: M013 Acetaminophen Extra Strength ACETAMINOPHEN Family Dollar Stores, LLC f86dcbb8-debc-4bce-e053-6294a90a7a02 2023-12-05 Warnings Exact identifier application number: M013 Sanatos Multi Symptom Daytime ACETAMINOPHEN, DEXTROMETHORPHAN HBR Pharmadel LLC 0a5fc0ef-ba34-bb0b-e063-6394a90af7d9 2023-12-01 Warnings Exact identifier application number: M013 Acetaminophen ACETAMINOPHEN Proficient Rx LP 402c8563-b14b-453f-80bc-4275f1c73702 2023-12-01 Warnings Exact identifier application number: M013 Acetaminophen and Diphenhydramine hydrochloride ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE Aurohealth LLC 3ba51b52-7ae6-4335-b178-1b7b6ef36227 2023-11-29 Warnings Exact identifier application number: M013 Acetaminophen Extra Strength ACETAMINOPHEN Aurohealth LLC bc03fa56-8880-4bbd-81a0-91853fecdd4e 2023-11-29 Warnings Exact identifier application number: M013
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 68071-3425-3 68071342503 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68071-3425-3) 2026-09-02 No No Current 68071-3425-9 68071342509 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68071-3425-9) 2023-06-01 No No Current