acetaminophen
- Product NDC
- 68788-0426
- 11-digit product format
- 687880426
- Labeler code
- 68788
- Product ID
- 68788-0426_b6e9e735-6335-4ddc-8d7e-1870f287e26c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- SUPPOSITORY
- Route
- RECTAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA070607
- Marketing category
- ANDA
- Marketing start
- 2010-12-14
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 120 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record