acetaminophen
- Product NDC
- 72162-2163
- 11-digit product format
- 721622163
- Labeler code
- 72162
- Product ID
- 72162-2163_1b702dd7-6704-48b6-8db0-ef115f23628c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-07-26
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 362O9ITL9D | ACETAMINOPHEN | 103-90-2 | ACETAMINOPHEN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2163-1 | 72162216301 | 100 TABLET in 1 BOTTLE (72162-2163-1) | 100 tablet | 2018-08-27 | No | No | Historical |