Up and Up Arthritis Pain Relief
- Product NDC
- 11673-210
- 11-digit product format
- 116730210
- Labeler code
- 11673
- Product ID
- 11673-210_b907568a-da53-4248-81b2-9956ad816191
- 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
- 2015-03-06
- Marketing end
- 2021-11-30
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-210-62 | 11673021062 | 1 BOTTLE in 1 CARTON (11673-210-62) > 24 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2015-03-06 | 0000-00-00 | No | No | Current |