Acetaminophen
- Product NDC
- 11822-0544
- 11-digit product format
- 118220544
- Labeler code
- 11822
- Product ID
- 11822-0544_eef9d3f7-a780-4fd4-a4eb-06b5b1a806f2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA075077
- Marketing category
- ANDA
- Marketing start
- 2013-09-30
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-0544-1 | 11822054401 | 1 BOTTLE in 1 CARTON (11822-0544-1) > 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2013-09-30 | 0000-00-00 | No | No | Current |
| 11822-0544-2 | 11822054402 | 1 BOTTLE in 1 CARTON (11822-0544-2) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2013-09-30 | 0000-00-00 | No | No | Current |
| 11822-0544-3 | 11822054403 | 1 BOTTLE in 1 CARTON (11822-0544-3) > 250 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2013-09-30 | 0000-00-00 | No | No | Current |
| 11822-0544-4 | 11822054404 | 225 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (11822-0544-4) | | 2013-09-30 | 0000-00-00 | No | No | Current |