TYLENOL
- Product NDC
- 50580-495
- 11-digit product format
- 505800495
- Labeler code
- 50580
- Product ID
- 50580-495_25b09044-067e-eb90-e063-6394a90a6d21
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Kenvue Brands LLC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-12-01
- Substance
- ACETAMINOPHEN
- Active strength
- 325 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- TYLENOL
- Brand name suffix
- Regular Strength
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 325 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 209387, 313782 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50580-495-01 | TYLENOLRegular Strength | 100 in 1 BOTTLE | TABLET | 100 | | 7 |
| 50580-495-01 | TYLENOLRegular Strength | 1 in 1 CARTON | TABLET | 1 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50580-495 | TYLENOL REGULAR STRENGTH (ACETAMINOPHEN) TABLET [KENVUE BRANDS LLC] | 7 | Current NDC, Legacy NDC, 2 package rows | 20241109_de5c6654-56c5-40d3-a286-f04ed47ac7c8.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 |
|---|
| 50580-495-01 | 50580049501 | 1 BOTTLE in 1 CARTON (50580-495-01) / 100 TABLET in 1 BOTTLE | 1 bottle | 2019-12-01 | 0000-00-00 | No | No | Current |