Acetaminophen
- Product NDC
- 11822-0631
- 11-digit product format
- 118220631
- Labeler code
- 11822
- Product ID
- 11822-0631_ac4477fe-74e6-4585-82d6-641c964e994c
- 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
- 2017-02-01
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 11822-0631-0 | 11822063100 | 1 BOTTLE in 1 CARTON (11822-0631-0) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2017-02-01 | 0000-00-00 | No | No | Current |
| 11822-0631-1 | 11822063101 | 1 BOTTLE in 1 CARTON (11822-0631-1) > 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2017-02-01 | 0000-00-00 | No | No | Current |