acetaminophen
- Product NDC
- 11822-0217
- 11-digit product format
- 118220217
- Labeler code
- 11822
- Product ID
- 11822-0217_d1bd1bd3-048a-4314-ac24-9b7f7885ede2
- 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
- 2013-09-21
- 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