equaline arthritis
- Product NDC
- 41163-544
- 11-digit product format
- 411630544
- Labeler code
- 41163
- Product ID
- 41163-544_b7eacff8-d8ed-40e9-9e31-eca15a534607
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Supervalu Inc
- Application
- ANDA075077
- Marketing category
- ANDA
- Marketing start
- 2012-08-29
- 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