Imiquimod
NDC 51672-4174 · Sun Pharmaceutical Industries, Inc.
Generic nameImiquimod
Dosage formCREAM
RouteTOPICAL
Active ingredient(s)IMIQUIMOD
Strength37.5 mg/g
Pharmacologic classIncreased Cytokine Activity [PE], Increased Cytokine Production [PE], Interferon Inducers [MoA]
Marketing categoryANDA
Packages
51672-4174-6 — 28 PACKET in 1 CARTON (51672-4174-6) / .25 g in 1 PACKET (51672-4174-8)
51672-4174-9 — 1 BOTTLE, PUMP in 1 CARTON (51672-4174-9) / 7.5 g in 1 BOTTLE, PUMP
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
0093-3133 — imiquimod, 45802-368 — Imiquimod, 51672-4145 — Imiquimod, 68462-536 — Imiquimod, 68682-272 — imiquimod, 71335-2725 — Imiquimod, 71335-3000 — Imiquimod, 72162-2332 — Imiquimod, 72189-084 — IMIQUIMOD, 99207-270 — imiquimod, 99207-271 — imiquimod, 99207-276 — imiquimod