TYLENOL Extra Strength
- Product NDC
- 50580-108
- 11-digit product format
- 505800108
- Labeler code
- 50580
- Product ID
- 50580-108_4d481f6b-0231-d4af-e063-6394a90ad1af
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Kenvue Brands LLC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-10-13
- 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
- TYLENOL Extra Strength
- 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, 209459 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50580-108-20 | TYLENOL Extra Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 2 |
| 50580-108-20 | TYLENOL Extra Strength | 200 in 1 BOTTLE | TABLET, FILM COATED | 200 | | 2 |
| 50580-108-25 | TYLENOL Extra Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 2 |
| 50580-108-25 | TYLENOL Extra Strength | 225 in 1 BOTTLE | TABLET, FILM COATED | 225 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50580-108-20 | 50580010820 | 1 in 1 CARTON | | | | | Historical |
| 50580-108-25 | 50580010825 | 1 BOTTLE in 1 CARTON (50580-108-25) / 225 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2025-10-13 | No | No | Current |