up and up acetaminophen
- Product NDC
- 11673-966
- 11-digit product format
- 116730966
- Labeler code
- 11673
- Product ID
- 11673-966_4b8472c3-8d40-41e5-8f4b-5f7615e4005c
- 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
- 2015-03-18
- 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 |
|---|
| 11673-966 | UP AND UP ACETAMINOPHEN (ACETAMINOPHEN) TABLET, FILM COATED, EXTENDED RELEASE [TARGET CORPORATION] | 3 | Legacy NDC | 20191213_842bf57f-cbd0-49c4-8c02-80f970ce0fc3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-966-78 | 11673096678 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (11673-966-78) | 2018-03-15 | 0000-00-00 | No | No | Current |