Regular Strength Pain Relief
- Product NDC
- 57896-104
- Requested package NDC
- 57896-104-01
- 11-digit product format
- 578960104
- Labeler code
- 57896
- Product ID
- 57896-104_ed992655-7882-1c08-e053-2995a90a5b94
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Geri-Care Pharmaceutical Corp
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-04-01
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 325 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 57896-104 | REGULAR STRENGTH PAIN RELIEF (ACETAMINOPHEN) TABLET [GERI-CARE PHARMACEUTICAL CORP] | 6 | Legacy NDC | 20231019_ac8abc37-5eb2-ae24-e053-2a95a90adc31.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 |
|---|
| 57896-104-01 | 57896010401 | 100 TABLET in 1 BOTTLE (57896-104-01) | 100 tablet | 2020-04-01 | 0000-00-00 | No | No | Current |