United States · FDA National Drug Code directory

Ritonavir

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
60687-420_160232e3-ff90-2a94-e063-6294a90a9a0c
Product NDC
60687-420
Form
TABLET, FILM COATED
Composition / generic term
Ritonavir
Labeler
American Health Packaging
Marketing category
ANDA
Marketing start / end (source format)
20181227
Source listing expiry
20261231

Source-listed ingredients

  • RITONAVIR — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-420-25) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-420-95) · 60687-420-25

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 →