Acetaminophen
- Product NDC
- 58602-866
- 11-digit product format
- 586020866
- Labeler code
- 58602
- Product ID
- 58602-866_53e7813e-e621-4166-b5c9-72cca45cd4f3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Aurohealth LLC
- Application
- ANDA207229
- Marketing category
- ANDA
- Marketing start
- 2022-10-19
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 362O9ITL9D | ACETAMINOPHEN | 103-90-2 | ACETAMINOPHEN |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58602-866-40 | 58602086640 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (58602-866-40) | 2022-10-19 | 0000-00-00 | No | No | Current |