Goodmeds Extra Strength Pain Relief Acetaminophen
- Product NDC
- 82725-4027
- 11-digit product format
- 827254027
- Labeler code
- 82725
- Product ID
- 82725-4027_47bae657-ada0-abd0-e063-6294a90a2d85
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACETAMINOPHEN
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cabinet Health P.B.C.
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-11-10
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Goodmeds Extra Strength Pain Relief Acetaminophen
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 198440 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 82725-4027-1 | Goodmeds Extra Strength Pain Relief Acetaminophen | 500 in 1 BOTTLE | TABLET | 500 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82725-4027-1 | 82725402701 | 500 TABLET in 1 BOTTLE (82725-4027-1) | 500 tablet | 2025-11-10 | No | No | Current |