Up and Up acetaminophen
- Product NDC
- 11673-618
- 11-digit product format
- 116730618
- Labeler code
- 11673
- Product ID
- 11673-618_e2b53c29-79b0-4335-816e-653c133feb4e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- ANDA075077
- Marketing category
- ANDA
- Marketing start
- 2017-03-02
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-618 | UP AND UP ACETAMINOPHEN (ACETAMINOPHEN) TABLET, FILM COATED, EXTENDED RELEASE [TARGET CORPORATION] | 3 | Legacy NDC | 20191213_a6b2603f-4cca-4fb8-9a16-6e4a6e2eec81.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-618-62 | 11673061862 | 1 BOTTLE in 1 CARTON (11673-618-62) > 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2017-03-02 | 0000-00-00 | No | No | Current |
| 11673-618-78 | 11673061878 | 1 BOTTLE in 1 CARTON (11673-618-78) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2017-03-02 | 0000-00-00 | No | No | Current |