Acetaminophen
- Product NDC
- 70000-0709
- 11-digit product format
- 700000709
- Labeler code
- 70000
- Product ID
- 70000-0709_2b4a2dd1-b832-acfc-e063-6394a90a0476
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- LEADER/ Cardinal Health 110, Inc.
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-12-10
- 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 |
|---|
| 70000-0709-1 | 70000070901 | 500 TABLET in 1 BOTTLE (70000-0709-1) | 500 tablet | 2024-12-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| 5427-Cardinal | LEADER/ Cardinal Health 110, Inc. | 2025-01-09 | HUMAN OTC DRUG LABEL | 8 |