United States · FDA National Drug Code directory
Pharbetol
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
- 71205-478_27ee285e-c641-4364-bd4a-7273b8e0cad2
- Product NDC
- 71205-478
- Form
- TABLET
- Composition / generic term
- Acetaminophen
- Labeler
- Proficient Rx LP
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20060110
- Source listing expiry
- 20261231
Source-listed ingredients
- ACETAMINOPHEN — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET in 1 BOTTLE, PLASTIC (71205-478-20) · 71205-478-20
- 24 TABLET in 1 BOTTLE, PLASTIC (71205-478-24) · 71205-478-24
- 30 TABLET in 1 BOTTLE, PLASTIC (71205-478-30) · 71205-478-30
- 40 TABLET in 1 BOTTLE, PLASTIC (71205-478-40) · 71205-478-40
- 50 TABLET in 1 BOTTLE, PLASTIC (71205-478-50) · 71205-478-50
- 60 TABLET in 1 BOTTLE, PLASTIC (71205-478-60) · 71205-478-60
- 90 TABLET in 1 BOTTLE, PLASTIC (71205-478-90) · 71205-478-90
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 →