United States · FDA National Drug Code directory
Acetaminophen
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 21130-108_dbcabfb5-6e41-4ffe-a78a-6633188332dc
- Product NDC
- 21130-108
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Acetaminophen
- Labeler
- Better Living Brands, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220624
- Source listing expiry
- 20271231
Source-listed ingredients
- ACETAMINOPHEN — 650 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (21130-108-07) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE · 21130-108-07
- 1 BOTTLE in 1 CARTON (21130-108-35) / 225 TABLET, EXTENDED RELEASE in 1 BOTTLE · 21130-108-35
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →