Acetaminophen
- Product NDC
- 41163-669
- 11-digit product format
- 411630669
- Labeler code
- 41163
- Product ID
- 41163-669_328d078e-240a-40f3-b23a-787bd72d2930
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- EQUALINE (SuperValu)
- Application
- ANDA207035
- Marketing category
- ANDA
- Marketing start
- 2019-09-30
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41163-669-10 | 41163066910 | 1 BOTTLE, PLASTIC in 1 BOX (41163-669-10) > 100 TABLET in 1 BOTTLE, PLASTIC | 2019-09-30 | 0000-00-00 | No | No | Current |
| 41163-669-50 | 41163066950 | 1 BOTTLE, PLASTIC in 1 BOX (41163-669-50) > 50 TABLET in 1 BOTTLE, PLASTIC | 2019-09-30 | 0000-00-00 | No | No | Current |