arthritis pain relief
- Product NDC
- 41250-544
- 11-digit product format
- 412500544
- Labeler code
- 41250
- Product ID
- 41250-544_0c850247-0dbc-4e1b-850f-a4e293bcbe3d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- ANDA075077
- Marketing category
- ANDA
- Marketing start
- 2005-03-26
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 650 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 41250-544-78 | 41250054478 | 1 BOTTLE in 1 CARTON (41250-544-78) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2005-03-26 | 0000-00-00 | No | No | Current |
| 41250-544-79 | 41250054479 | 400 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (41250-544-79) | | 2015-04-07 | 0000-00-00 | No | No | Current |
| 41250-544-83 | 41250054483 | 1 BOTTLE in 1 CARTON (41250-544-83) > 225 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2017-05-08 | 0000-00-00 | No | No | Current |
| 41250-544-85 | 41250054485 | 1 BOTTLE in 1 CARTON (41250-544-85) > 250 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2005-04-10 | 0000-00-00 | No | No | Current |