Extra Strength Pain Relief
- Product NDC
- 82501-1575
- 11-digit product format
- 825011575
- Labeler code
- 82501
- Product ID
- 82501-1575_ee17d117-e437-f5a6-e053-2a95a90a918b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Gobrands, Inc
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-05-11
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 82501-1575-1 | Extra Strength Pain Relief | 100 in 1 BOTTLE | TABLET, COATED | 100 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82501-1575 | EXTRA STRENGTH PAIN RELIEF (ACETAMINOPHEN) TABLET, COATED [GOBRANDS, INC] | 5 | Legacy NDC, 1 package rows | 20241222_0ec56ff0-e848-422c-96ec-03d1d95fdf0a.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 |
|---|
| 82501-1575-1 | 82501157501 | 100 TABLET, COATED in 1 BOTTLE (82501-1575-1) | 2022-05-11 | 0000-00-00 | No | No | Current |