Aspirin 325 mg
- Product NDC
- 41250-681
- Requested package NDC
- 41250-681-02
- 11-digit product format
- 412500681
- Labeler code
- 41250
- Product ID
- 41250-681_9522c328-6502-7d01-e053-2995a90a2b33
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aspirin
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Meijer
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-06-01
- Marketing end
- 0000-00-00
- Substance
- ASPIRIN
- Active strength
- 325 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 41250-681 | 41250-681-02 | D | Discontinued by firm | 2026-10-15 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 41250-681-02 | 41250068102 | 1 BOTTLE, PLASTIC in 1 PACKAGE (41250-681-02) > 125 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC | 2017-06-01 | 0000-00-00 | No | No | Current |