acetaminophen
- Product NDC
- 71335-2251
- 11-digit product format
- 713352251
- Labeler code
- 71335
- Product ID
- 71335-2251_8add73d8-1f71-45c6-9ff7-cf71a7ae9029
- 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
Additional Listing Data
- Finished product
- Yes
- Brand name base
- acetaminophen
- Listing expiration
- 2026-12-31
Active Ingredients
| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 500 mg/1 |
Harmonized Identifiers
| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 198440 |
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 |
|---|
| 71335-2251-1 | 71335225101 | 30 TABLET in 1 BOTTLE (71335-2251-1) | 30 tablet | 2024-11-01 | No | No | Historical |