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
62207-183_5447f567-0cef-ae0a-e063-6394a90ad867
Product NDC
62207-183
Form
TABLET, EXTENDED RELEASE
Composition / generic term
ACETAMINOPHEN
Labeler
Granules India Limited
Marketing category
ANDA
Marketing start / end (source format)
20190418
Source listing expiry
20271231

Source-listed ingredients

  • ACETAMINOPHEN — 650 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 POUCH in 1 BOX (62207-183-34) / 5 TABLET, EXTENDED RELEASE in 1 POUCH · 62207-183-34
  • 6 POUCH in 1 BOX (62207-183-35) / 3000 TABLET, EXTENDED RELEASE in 1 POUCH · 62207-183-35
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62207-183-49) · 62207-183-49
  • 1 BOTTLE in 1 CARTON (62207-183-51) / 10 TABLET, EXTENDED RELEASE in 1 BOTTLE · 62207-183-51
  • 1 POUCH in 1 BOX (62207-183-87) / 1 TABLET, EXTENDED RELEASE in 1 POUCH · 62207-183-87
  • 40000 TABLET, EXTENDED RELEASE in 1 DRUM (62207-183-97) · 62207-183-97

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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