LOW DOSE ASPIRIN
- Product NDC
- 50090-4830
- 11-digit product format
- 500904830
- Labeler code
- 50090
- Product ID
- 50090-4830_05ef1eaa-c8f8-433a-9151-eecc565241b6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ASPIRIN
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2015-06-19
- 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
- 2026-12-31
- 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
- LOW DOSE ASPIRIN
- Listing expiration
- 2026-12-31
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 |
|---|---|
| ee4451c9-4d0f-4373-8f64-fcc1f9dd5856 | 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 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Related label |
|---|---|---|
| 50090-4830-1 | 2024-02-29 | 481R TCL 49483-481 ASPIRIN 81MG DELAYED RELEASE TABLETS |
| 50090-4830-2 | 2024-02-29 | 481R TCL 49483-481 ASPIRIN 81MG DELAYED RELEASE TABLETS |
| 50090-4830-3 | 2024-02-29 | 481R TCL 49483-481 ASPIRIN 81MG DELAYED RELEASE TABLETS |
| 50090-4830-1 | 2023-01-30 | 481R TCL 49483-481 ASPIRIN 81MG DELAYED RELEASE TABLETS |
| 50090-4830-2 | 2023-01-30 | 481R TCL 49483-481 ASPIRIN 81MG DELAYED RELEASE TABLETS |
| 50090-4830-3 | 2023-01-30 | 481R TCL 49483-481 ASPIRIN 81MG DELAYED RELEASE TABLETS |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50090-4830-1 | LOW DOSE ASPIRIN | 120 in 1 BOTTLE | TABLET, COATED | 120 | 12 | |
| 50090-4830-2 | LOW DOSE ASPIRIN | 30 in 1 BOTTLE | TABLET, COATED | 30 | 12 | |
| 50090-4830-3 | LOW DOSE ASPIRIN | 90 in 1 BOTTLE | TABLET, COATED | 90 | 12 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50090-4830-1 | EA - Each | 50090-4830 | a7f9f149-a821-43cd-b75f-8e8cfc2f7959 | 1 | 2022-12-07 |
| 50090-4830-3 | EA - Each | 50090-4830 | 6005bdef-c9bb-4ef5-8d39-6b61fc053ecd | 1 | 2023-09-05 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50090-4830 | LOW DOSE ASPIRIN (ASPIRIN) TABLET, COATED [A-S MEDICATION SOLUTIONS] | 12 | Current NDC, Legacy NDC, 3 package rows | 20240229_ee4451c9-4d0f-4373-8f64-fcc1f9dd5856.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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Aspirin | ASPIRIN | Proficient Rx LP | 9c186289-e309-45e8-8934-1d0eae0375c2 | 2024-12-01 | Warnings | M013 |
| Childrens Chewable Acetaminophen | ACETAMINOPHEN | GERI-CARE PHARMACEUTICAL CORP | 22f63d62-c941-5b8f-e063-6394a90aeecd | 2024-11-28 | Warnings | M013 |
| Extra Strength Acetaminophen | ACETAMINOPHEN | Geri-Care Pharmaceutical Corp | 7a7b6318-b7d6-31b1-e053-2991aa0abf25 | 2024-11-28 | Warnings | M013 |
| Extra Strength Pain Reliever PM | ACETAMINOPHEN, DIPHENHYDRAMINE HCL | INGLES MARKETS, INC. | 27fd288e-c07a-617f-e063-6394a90a17a4 | 2024-11-28 | Warnings | M013 |
| BAYER Aspirin Original, TRAVEL BASIX | ASPIRIN | Lil' Drug Store Products, Inc. | 7f5d9ebe-8119-49a2-9380-eca18a5e5e85 | 2024-11-27 | Warnings | M013 |
| EXCEDRIN MIGRAINE | ACETAMINOPHEN, ASPIRIN (NSAID) AND CAFFEINE | Jones Healthcare Group - Packaging Services, Inc | c4168e4d-3dfc-4e51-a32e-14704cb59c66 | 2024-11-27 | Warnings | M013 |
| TYLENOL Extra Strength / TYLENOL Precise Cooling Pain Relief | ACETAMINOPHEN, LIDOCAINE, MENTHOL | Kenvue Brands LLC | 2611e984-0dd5-bda1-e063-6394a90a559a | 2024-11-26 | Warnings | M013 |
| First Aid Only Extra-Strength Non-Aspirin | ACETAMINOPHEN | Acme United Corporation | 6891d57a-10a6-53de-e053-2a91aa0ac7c2 | 2024-11-26 | Warnings | M013 |
| Chewable Aspirin | ASPIRIN | MARC GLASSMAN, INC. | c8314910-71ff-5a55-e053-2995a90aafc7 | 2024-11-26 | Warnings | M013 |
| Aspirin | ASPIRIN | Marc Glassman, Inc. | 7990ca49-fb30-40fe-9ac4-48e89eac9bb2 | 2024-11-26 | Warnings | M013 |
| Enteric Coated Aspirin Regular Strength | ASPIRIN | Safeway | 96359eb6-62bc-4b13-960c-050af99a8c02 | 2024-11-26 | Warnings | M013 |
| ASPIRIN Low Dose | ASPIRIN | Marc Glassman, Inc. | 3d519af3-9398-4439-8253-1e5d4612b8e3 | 2024-11-26 | Warnings | M013 |
| ACETAMINOPHEN (RED) | ACETAMINOPHEN | Humanwell PuraCap Pharmaceutical (Wuhan), Ltd. | 06eabf4b-f8c0-439a-acf1-aa6e3075c717 | 2024-11-25 | Warnings | M013 |
| ACETAMINOPHEN (RED) | ACETAMINOPHEN | Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd | a352f588-4a70-42b2-8f9c-a73a0629517d | 2024-11-25 | Warnings | M013 |
| Pain Relief Extra Strength | ACETAMINOPHEN | Humanwell PuraCap Pharmaceutical (Wuhan), Ltd. | 5c42dd28-820c-4cc5-9016-11ad5e580616 | 2024-11-25 | Warnings | M013 |
| equate pain reliever | ACETAMINOPHEN | WALMART INC. | 4518fe82-3ba8-4e9e-a036-776df7fb8d57 | 2024-11-21 | Warnings | M013 |
| Family Wellness Pain Reliever | ASPIRIN | FAMILY WELLNESS SERVICES, INC. | 075e19f4-1a58-aedd-e063-6294a90af708 | 2024-11-20 | Warnings | M013 |
| Mejoralito | ACETAMINOPHEN | OPMX Chula Vista | fd2ecde0-296e-060f-e053-6294a90afd98 | 2024-11-15 | Warnings | M013 |
| Temp X | ACETAMINOPHEN | OPMX Chula Vista | fd2edc32-0351-c991-e053-6294a90ab4ce | 2024-11-15 | Warnings | M013 |
| CVS Health Extra Strength Antacid and Pain Reliever | ASPIRIN, ANHYDROUS CITRIC ACID, SODIUM BICARBONATE | CVS Pharmacy | afe9e755-18ba-305f-e053-2995a90aa8d0 | 2024-11-14 | Warnings | M013 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 308416 | aspirin 81 MG Delayed Release Oral Tablet | PSN | ee4451c9-4d0f-4373-8f64-fcc1f9dd5856 | 12 |
| 308416 | aspirin 81 MG Delayed Release Oral Tablet | SCD | ee4451c9-4d0f-4373-8f64-fcc1f9dd5856 | 12 |
| 308416 | ASA 81 MG Delayed Release Oral Tablet | SY | ee4451c9-4d0f-4373-8f64-fcc1f9dd5856 | 12 |
| 308416 | aspirin 81 MG Enteric Coated Oral Tablet | SY | ee4451c9-4d0f-4373-8f64-fcc1f9dd5856 | 12 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 50090-4830-1 | 50090483001 | 120 TABLET, COATED in 1 BOTTLE (50090-4830-1) | 2020-01-09 | 0000-00-00 | No | No | Current |
| 50090-4830-2 | 50090483002 | 30 TABLET, COATED in 1 BOTTLE (50090-4830-2) | 2020-01-09 | 0000-00-00 | No | No | Current |
| 50090-4830-3 | 50090483003 | 90 TABLET, COATED in 1 BOTTLE (50090-4830-3) | 2020-01-09 | 0000-00-00 | No | No | Current |