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RETROVIR

NDC 49702-212 · ViiV Healthcare Company

Generic namezidovudine
Dosage formSOLUTION
RouteORAL
Active ingredient(s)ZIDOVUDINE
Strength10 mg/mL
Pharmacologic classHuman Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Nucleoside Reverse Transcriptase Inhibitors [MoA]
Marketing categoryNDA

Packages

49702-212-48 — 240 mL in 1 BOTTLE (49702-212-48)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

31722-506 — LAMIVUDINE and ZIDOVUDINE, 31722-509 — Zidovudine, 31722-739 — Lamivudine and Zidovudine, 33342-003 — Lamivudine and Zidovudine, 43063-900 — LAMIVUDINE and ZIDOVUDINE, 49702-202 — lamivudine and zidovudine, 49702-211 — zidovudine, 49702-213 — zidovudine, 65862-024 — Zidovudine, 65862-036 — Lamivudine and Zidovudine, 65862-048 — Zidovudine, 65862-107 — Zidovudine, 67046-1613 — Zidovudine, 68180-286 — ABACAVIR , LAMIVUDINE AND ZIDOVUDINE, 71335-0639 — LAMIVUDINE and ZIDOVUDINE, 71335-1916 — Lamivudine and Zidovudine, 72865-144 — lamivudine and zidovudine, 76282-115 — Lamivudine and Zidovudine

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.