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
- 49483-699_02a5f067-4b67-ecc7-e063-6294a90a92c3
- Product NDC
- 49483-699
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Acetaminophen tablet extended release
- Labeler
- TIME CAP LABORATORIES, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211004
- Source listing expiry
- 20261231
Source-listed ingredients
- ACETAMINOPHEN — 650 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (49483-699-01) · 49483-699-01
- 50 BOTTLE in 1 CARTON (49483-699-05) / 1 TABLET, EXTENDED RELEASE in 1 BOTTLE · 49483-699-05
- 225 TABLET, EXTENDED RELEASE in 1 BOTTLE (49483-699-26) · 49483-699-26
- 400 TABLET, EXTENDED RELEASE in 1 BOTTLE (49483-699-40) · 49483-699-40
- 1 BOTTLE in 1 CARTON (49483-699-42) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE · 49483-699-42
Source and coverage
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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.
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