EXTRA STRENGTH ACETAMINOPHEN
- Product NDC
- 68210-6113
- Requested package NDC
- 68210-6113-1
- 11-digit product format
- 682106113
- Labeler code
- 68210
- Product ID
- 68210-6113_ee27959f-6e73-d753-e053-2a95a90a81b0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACETAMINOPHEN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Spirit Pharmaceutical LLC
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-04-06
- 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 Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68210-6113-1 | EXTRA STRENGTH ACETAMINOPHEN | 1 in 1 CARTON | TABLET | 1 | | 6 |
| 68210-6113-1 | EXTRA STRENGTH ACETAMINOPHEN | 100 in 1 BOTTLE | TABLET | 100 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68210-6113 | EXTRA STRENGTH ACETAMINOPHEN (ACETAMINOPHEN) TABLET [SPIRIT PHARMACEUTICAL LLC] | 6 | Legacy NDC, 2 package rows | 20241222_dca3f1b7-004f-4972-95dc-efeacfb4cb32.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68210-6113-1 | 68210611301 | 1 BOTTLE in 1 CARTON (68210-6113-1) > 100 TABLET in 1 BOTTLE | 1 bottle | 2020-04-06 | 0000-00-00 | No | No | Current |