Tylenol
- Product NDC
- 50580-487
- 11-digit product format
- 505800487
- Labeler code
- 50580
- Product ID
- 50580-487_774ddbe6-eb0c-4efd-b7aa-5c17058d58bb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2016-01-05
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 325 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50580-487-20 | 50580048720 | 1 BOTTLE in 1 CARTON (50580-487-20) > 20 CAPSULE, LIQUID FILLED in 1 BOTTLE | 1 bottle | 2016-01-05 | 0000-00-00 | No | No | Current |
| 50580-487-90 | 50580048790 | 1 BOTTLE in 1 CARTON (50580-487-90) > 90 CAPSULE, LIQUID FILLED in 1 BOTTLE | 1 bottle | 2016-01-05 | 0000-00-00 | No | No | Current |