United States · FDA National Drug Code directory
LAMIVUDINE AND ZIDOVUDINE
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
- 72865-144_f26f80c3-6ad3-2c78-e053-2995a90a7783
- Product NDC
- 72865-144
- Form
- TABLET, FILM COATED
- Composition / generic term
- lamivudine and zidovudine
- Labeler
- XLCare Pharmaceuticals, Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200417
- Source listing expiry
- 20261231
Source-listed ingredients
- LAMIVUDINE — 150 mg/1
- ZIDOVUDINE — 300 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, FILM COATED in 1 BOTTLE (72865-144-60) · 72865-144-60
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 →