Aspirin 81 mg
- Product NDC
- 42507-080
- 11-digit product format
- 425070080
- Labeler code
- 42507
- Product ID
- 42507-080_48494033-500a-1348-e063-6394a90a8cb2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ASPIRIN
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- HYVEE INC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-10-22
- 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
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 81 mg
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ASPIRIN | 81 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| R16CO5Y76E | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 308416 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 3e602287-565e-a5b9-e063-6294a90abc17 | Available on FDA.report |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| d7724692-1155-4cc8-a415-22f5fc4aec35 | Product name | 6 | 20220216 |
| bde672ba-4805-28d0-1986-73543d41b412 | Product name | 2 | 20210201 |
| f212291f-05fe-9603-fc7e-bd73e38ce1e6 | Product name | 2 | 20161129 |
| ade821ba-260a-47e2-bd89-743e27ac9906 | Product name | 1 | 20161121 |
| 182f9ab4-4ab5-c449-200f-87ce2ce8e550 | Product name | 2 | 20151105 |
| 9425d234-4ae1-4b53-adc6-8cc7af6dd657 | Product name | 1 | 20150929 |
| 2a21311a-89e2-0e83-2ebd-117f9798b2b2 | Product name | 1 | 20140508 |
| 9007e8a7-ff50-f9b9-7945-f2a1deadd94e | Product name | 1 | 20140508 |
| 96c2be53-8e44-452d-56a2-d255b2f1af2d | Product name | 1 | 20140508 |
| bf8bd5f7-495f-4022-2780-7ded7ea7ea44 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 42507-080-01 | Aspirin 81 mg | 120 in 1 BOTTLE, PLASTIC | TABLET, DELAYED RELEASE | 120 | 3 | |
| 42507-080-01 | Aspirin 81 mg | 120 in 1 CARTON | TABLET, DELAYED RELEASE | 120 | 3 | |
| 42507-080-04 | Aspirin 81 mg | 500 in 1 BOTTLE, PLASTIC | TABLET, DELAYED RELEASE | 500 | 3 | |
| 42507-080-08 | Aspirin 81 mg | 2 in 1 CARTON | TABLET, DELAYED RELEASE | 2 | 3 | |
| 42507-080-08 | Aspirin 81 mg | 120 in 1 BOTTLE, PLASTIC | TABLET, DELAYED RELEASE | 120 | 3 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Extra Strength Pain Relief PM | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE | VALU MERCHANDISERS COMPANY | f8820150-feec-4062-85bb-14525ddf691f | 2025-12-11 | Warnings | M013 |
| Extra Strength Pain Relief | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | 005e299e-aa84-49d9-bbca-12236f865a27 | 2025-12-11 | Warnings | M013 |
| Low Dose Chewable Aspirin | ASPIRIN | VALU MERCHANDISERS COMPANY | 7d88f156-d361-4249-b70d-4bbcd5ba30b7 | 2025-12-11 | Warnings | M013 |
| Enteric Coated Aspirin | ASPIRIN | VALU MERCHANDISERS COMPANY | cc18e8e1-652e-44da-a9d7-e56cebda55a1 | 2025-12-11 | Warnings | M013 |
| Extra Strength Pain Relief | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | d4c32e70-778a-4d66-b9d0-03944a528421 | 2025-12-11 | Warnings | M013 |
| adult low dose aspirin | ASPIRIN | VALU MERCHANDISERS COMPANY | 6fa1c707-bd42-455b-90a3-2c2a11acc683 | 2025-12-11 | Warnings | M013 |
| Extra Strength Pain Relief | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | 5a80cb17-7731-4457-acd3-64cf4accf862 | 2025-12-11 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | 02e3798f-86d9-64b4-e063-6294a90a29de | 2025-12-11 | Warnings | M013 |
| Regular Strength Pain Relief | ACETAMINOPHEN | VALU MERCHANDISERS COMPANY | f7e87eac-59fb-4a72-b5c6-02953112be6a | 2025-12-11 | Warnings | M013 |
| Aspirin | ASPIRIN | VALU MERCHANDISERS COMPANY | 049ec1aa-66b3-9273-e063-6294a90a221b | 2025-12-11 | Warnings | M013 |
| Aspirin 325 | ASPIRIN | Walgreen Company | f7a5d612-443c-4701-ad3b-8eb53c87bece | 2025-12-11 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | PAI Holdings, LLC dba PAI Pharma | 355a094c-bed9-4959-8cf0-619f0e246105 | 2025-12-11 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | PAI Holdings, LLC dba PAI Pharma | fac4e0c6-684f-45a1-99f2-de4de4017cc8 | 2025-12-11 | Warnings | M013 |
| Pain Reliever PM extra strength | ACETAMINOPHEN DIPHENHYDRAMINE HCL | P & L Development, LLC | 90eba2e8-52c3-43f5-ba93-4a520368c7f4 | 2025-12-11 | Warnings | M013 |
| Midol Complete, Travel BASIX | ACETAMINOPHEN, CAFFEINE, AND PYRILAMINE MALEATE | Lil' Drug Store Products, Inc | d6d47af8-5f8c-4c8c-a8c6-aa214ec23bca | 2025-12-10 | Warnings | M013 |
| Tylenol PM Extra Strength, CVP HEALTH | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE | Lil' Drug Store Products, Inc. | 643371f2-e330-441e-8932-b3aec4b179d2 | 2025-12-10 | Warnings | M013 |
| Low Dose Aspirin | ASPIRIN | United Natural Foods, Inc. dba UNFI | 18b79449-5c4c-41ce-9609-80f5efa0375c | 2025-12-09 | Warnings | M013 |
| Pain Relief | ACETAMINOPHEN | AAA Pharmaceutical, Inc. | 36ad34f4-4e66-f371-e063-6394a90ae76a | 2025-12-09 | Warnings | M013 |
| Pain Reliever | ACETAMINOPHEN | LIDL US LLC | ec543339-20ab-2cba-e053-2995a90ac740 | 2025-12-09 | Warnings | M013 |
| Pain Relief Extra Strength | ACETAMINOPHEN | CHAIN DRUG MARKETING ASSOCIATION, INC. | c57c10fc-f182-4153-8974-ef359a5f5ac1 | 2025-12-09 | Warnings | M013 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 308416 | aspirin 81 MG Delayed Release Oral Tablet | PSN | 3e602287-565e-a5b9-e063-6294a90abc17 | 3 |
| 308416 | aspirin 81 MG Delayed Release Oral Tablet | SCD | 3e602287-565e-a5b9-e063-6294a90abc17 | 3 |
| 308416 | ASA 81 MG Delayed Release Oral Tablet | SY | 3e602287-565e-a5b9-e063-6294a90abc17 | 3 |
| 308416 | aspirin 81 MG Enteric Coated Oral Tablet | SY | 3e602287-565e-a5b9-e063-6294a90abc17 | 3 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|
| 42507-080-01 | 42507008001 | 120 in 1 BOTTLE, PLASTIC | Historical | |||
| 42507-080-04 | 42507008004 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (42507-080-04) | 2026-01-13 | No | No | Current |
| 42507-080-08 | 42507008008 | 2 BOTTLE, PLASTIC in 1 CARTON (42507-080-08) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC | 2025-10-22 | No | No | Current |