Tretinoin
NDC 51672-1407 · Sun Pharmaceutical Industries, Inc.
Generic nametretinoin
Dosage formCREAM
RouteTOPICAL
Active ingredient(s)TRETINOIN
Strength.25 mg/g
Pharmacologic classRetinoid [EPC], Retinoids [CS]
Marketing categoryANDA
Packages
51672-1407-0 — 1 TUBE in 1 CARTON (51672-1407-0) / 20 g in 1 TUBE
51672-1407-9 — 1 TUBE in 1 CARTON (51672-1407-9) / 45 g in 1 TUBE
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
46708-808 — Tretinoin, 46708-809 — Tretinoin, 50090-0651 — Tretinoin, 50090-3058 — tretinoin, 50090-3128 — tretinoin, 50090-4347 — tretinoin, 50090-6819 — tretinoin, 50090-7171 — tretinoin, 51672-1394 — tretinoin, 51672-1395 — tretinoin, 51862-771 — Benzoyl Peroxide and Tretinoin, 59651-712 — Tretinoin, 59651-713 — Tretinoin, 62032-412 — tretinoin, 62032-413 — Tretinoin, 62032-414 — tretinoin, 62032-417 — tretinoin, 62332-807 — Tretinoin, 62332-808 — Tretinoin, 62332-809 — Tretinoin, +70 more