Aspirin
- Product NDC
- 49638-102
- 11-digit product format
- 496380102
- Labeler code
- 49638
- Product ID
- 49638-102_c7429a4f-4710-2c68-e053-2a95a90ab3a0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aspirin
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- America Medic & Science, LLC
- Application
- part343
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-06-29
- Marketing end
- 0000-00-00
- Substance
- ASPIRIN
- Active strength
- 81 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.
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49638-102 | ASPIRIN TABLET, DELAYED RELEASE [AMERICA MEDIC & SCIENCE, LLC] | 8 | Legacy NDC | 20240206_88cb580d-64ec-4762-be76-71cccdc07f18.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49638-102-60 | 49638010260 | 1 BOTTLE in 1 CARTON (49638-102-60) > 60 TABLET, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2021-06-29 | 0000-00-00 | No | No | Current |