Aspirin
- Product NDC
- 80136-904
- Requested package NDC
- 80136-904-01
- 11-digit product format
- 801360904
- Labeler code
- 80136
- Product ID
- 80136-904_ce2cf84d-b23e-9d39-e053-2a95a90a12da
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aspirin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NORTHEAST PHARMA
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-09-01
- Marketing end
- 0000-00-00
- Substance
- ASPIRIN
- Active strength
- 325 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 80136-904-01 | Aspirin | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80136-904 | ASPIRIN TABLET, FILM COATED [NORTHEAST PHARMA] | 2 | Legacy NDC, 1 package rows | 20231027_ce2ceb93-2349-4a10-e053-2995a90ae9d5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80136-904-01 | 80136090401 | 100 TABLET, FILM COATED in 1 BOTTLE (80136-904-01) | 2020-09-01 | 0000-00-00 | No | No | Current |