Pain Relief
- Product NDC
- 37808-455
- 11-digit product format
- 378080455
- Labeler code
- 37808
- Product ID
- 37808-455_8949b031-6e7c-4a85-bd5c-0a9c58aac379
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- H E B
- Application
- ANDA075077
- Marketing category
- ANDA
- Marketing start
- 2005-10-01
- 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