United States · FDA National Drug Code directory

RETROVIR

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
49702-213_01ba4f9b-3d72-4bc2-bae1-ecb13a8b845a
Product NDC
49702-213
Form
INJECTION, SOLUTION
Composition / generic term
zidovudine
Labeler
ViiV Healthcare Company
Marketing category
NDA
Marketing start / end (source format)
20101104
Source listing expiry
20261231

Source-listed ingredients

  • ZIDOVUDINE — 10 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 5 VIAL, SINGLE-USE in 1 CARTON (49702-213-26) / 20 mL in 1 VIAL, SINGLE-USE (49702-213-01) · 49702-213-26

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.

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