Aspirin
- Product NDC
- 37835-577
- Requested package NDC
- 37835-577-01
- 11-digit product format
- 378350577
- Labeler code
- 37835
- Product ID
- 37835-577_5f86a3b1-d1cc-0d99-e063-6294a90a6914
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aspirin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bi-Mart
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-08-01
- Substance
- ASPIRIN
- Active strength
- 325 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
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ASPIRIN | 325 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| R16CO5Y76E | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 212033 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| cc5db55a-a2b0-48f4-802b-9e5e94fd9ceb | 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 |
|---|---|---|---|---|---|---|
| 37835-577-01 | Aspirin | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 1 | |
| 37835-577-25 | Aspirin | 250 in 1 BOTTLE | TABLET, FILM COATED | 250 | 1 |
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 Regimen | ASPIRIN | Cardinal Health 110, LLC. DBA Leader | 88f425df-712d-4911-824b-94085c7190b6 | 2026-06-19 | Warnings | M013 |
| Aspirin Low Dose | ASPIRIN | Meijer Distribution, Inc. | 3716a7d4-a555-4e54-aa0a-7b8f3e32addb | 2026-06-19 | Warnings | M013 |
| Pain Relief | ACETAMINOPHEN | DOLGENCORP, LLC | acc94a3e-21b6-4375-9881-38cf9bab8692 | 2026-06-19 | Warnings | M013 |
| Aspirin Low Dose | ASPIRIN | L.N.K. International, Inc. | 2f6ec676-3832-420e-be91-fce83f6586c8 | 2026-06-19 | Warnings | M013 |
| Headache Relief | ACETAMINOPHEN, ASPIRIN, CAFFEINE | DOLGENCORP, LLC | e1e24d52-0b4d-400b-8181-e3f6ab75c4f6 | 2026-06-18 | Warnings | M013 |
| Acetaminophen | ACETAMINOPHEN | Oncor Pharmaceuticals | 4c396d0e-aa93-4f9e-b065-2e606f7f05cd | 2026-06-17 | Warnings | M013 |
| LOW DOSE ASPIRIN | ASPIRIN | Famora Inc. | 4dc6f119-bbde-db5f-e063-6294a90a9486 | 2026-06-16 | Warnings | M013 |
| Childrens Pain and Fever Relief | ACETAMINOPHEN | Chain Drug Marketing Association, Inc. | 420a1e05-caa6-481f-bdab-a670f0220f96 | 2026-06-16 | Warnings | M013 |
| Pain Relief Extra Strength | ACETAMINOPHEN | DOLGENCORP, LLC | ce9f4e0d-43fb-499a-b8a2-a997a14841c4 | 2026-06-16 | Warnings | M013 |
| Pain Reliever | ACETAMINOPHEN | L.N.K. International, Inc. | 734cc3d2-6fc5-4dcc-93ed-0b57c1f01345 | 2026-06-15 | Warnings | M013 |
| RIGHT REMEDIES EXTRA STRENGTH Pain Relief PM Caplet | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE | Strive Pharmaceuticals Inc. | 2d63671d-cf7c-bbdd-e063-6294a90affef | 2026-06-15 | Warnings | M013 |
| TYLENOL Extra Strength | ACETAMINOPHEN | Kenvue Brands LLC | 59773893-09a8-47a2-943a-e9ea9da4458a | 2026-06-15 | Warnings | M013 |
| Pain Relief | ACETAMINOPHEN | Shield Pharmaceuticals Corp. | 96eb7f9f-ff2d-4661-bbe6-1860aafe03f6 | 2026-06-15 | Warnings | M013 |
| Duralgina Extra Strength | ACETAMINOPHEN | Menper Distributors, Inc. | 544e3d7e-a759-384f-e063-6294a90a5baa | 2026-06-15 | Warnings | M013 |
| pain relief childrens | ACETAMINOPHEN | Rite Aid Corporation | be2286a1-946b-4bf5-b14c-8e86da669594 | 2026-06-15 | Warnings | M013 |
| Aspirin 81 | ASPIRIN | Amerisource Bergen | 4491faca-f30b-4eb0-bea9-f518f6b2f095 | 2026-06-15 | Warnings | M013 |
| Headache Relief Extra Strength | ACETAMINOPHEN, ASPIRIN, CAFFEINE | P & L Development, LLC | 55e996cd-ef22-4e09-a05c-8aa994e4540b | 2026-06-12 | Warnings | M013 |
| CHILDRENS TYLENOL | ACETAMINOPHEN | Kenvue Brands LLC | 3162733b-9382-39f1-e063-6294a90ac420 | 2026-06-12 | Warnings | M013 |
| Acetaminophen Extra Strength | ACETAMINOPHEN | Dr. Reddy's Laboratories Inc. | 9769e0c0-2f4c-3b7a-1a65-c98fbce11681 | 2026-06-12 | Warnings | M013 |
| ACETAMINOPHEN | ACETAMINOPHEN | NuCare Pharmaceuticals, Inc. | 54010ddf-25d1-2016-e063-6294a90a877d | 2026-06-11 | Warnings | M013 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 212033 | aspirin 325 MG Oral Tablet | PSN | cc5db55a-a2b0-48f4-802b-9e5e94fd9ceb | 1 |
| 212033 | aspirin 325 MG Oral Tablet | SCD | cc5db55a-a2b0-48f4-802b-9e5e94fd9ceb | 1 |
| 212033 | ASA 325 MG Oral Tablet | SY | cc5db55a-a2b0-48f4-802b-9e5e94fd9ceb | 1 |
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|
| 37835-577-01 | 37835057701 | 100 TABLET, FILM COATED in 1 BOTTLE (37835-577-01) | 2025-08-01 | No | No | Current |